Platform Engineer - Up to 75K - Manchester - Hybrid (once a week in office) - Healthcare Plans, Community Days, Team Socials We are looking for a highly motivated Platform Engineer / Cloud Engineer to join an award-winning platform who within both the public and private sectors with offices in /Manchester and London. The technical team is comprised of over 30 individuals including Developers, Software Testers, DevOps, Product owners and Project Managers. This exciting opportunity will suit a talented and experienced Platform Engineer who is well versed in GCP / Google Cloud or AWS. The organisation employs over 80 people, expanding exponentially over the last few year including expansion into America. They are a big believer in sharing thoughts and encouraging and supporting innovation and creativity. The Platform Engineer will also be given the chance to be involved in all aspects of the project process from conception through to completion and launch. The environment is relaxed yet professional, gone are the days of a corporate rigid structure. The position is hybrid with 1 day in office and 4 days from home. Platform Engineer Experience Linux operating systems, Debian and RHEL/Centos Google Cloud Platform (GCP) or AWS Infrastructure as Code best practises (Terraform) Configuration Management - Ansible, Puppet, Packer Containerization - Docker & Kubernetes Knowledge of Continuous Integration processes - Jenkins and GitHub Scripting/programming languages (Python, Bash, Perl or Golang) Databases (primarily MySQL) DNs would also be beneficial (Fastly) We are not expecting the Platform Engineer to be an expert in everything above, just a strong basis knowledge and passion to learn more! You will be an enthusiastic Platform Engineer, a great communicator and have an inquisitive attitude. The successful Platform Engineer should have strong problem-solving abilities, organisational skills, and the ability to work as part of a team. We are interviewing currently so apply now for immediate consideration for the Platform Engineer position or contact George Harvey at ITSS Recruitment for further information.
Mar 22, 2025
Full time
Platform Engineer - Up to 75K - Manchester - Hybrid (once a week in office) - Healthcare Plans, Community Days, Team Socials We are looking for a highly motivated Platform Engineer / Cloud Engineer to join an award-winning platform who within both the public and private sectors with offices in /Manchester and London. The technical team is comprised of over 30 individuals including Developers, Software Testers, DevOps, Product owners and Project Managers. This exciting opportunity will suit a talented and experienced Platform Engineer who is well versed in GCP / Google Cloud or AWS. The organisation employs over 80 people, expanding exponentially over the last few year including expansion into America. They are a big believer in sharing thoughts and encouraging and supporting innovation and creativity. The Platform Engineer will also be given the chance to be involved in all aspects of the project process from conception through to completion and launch. The environment is relaxed yet professional, gone are the days of a corporate rigid structure. The position is hybrid with 1 day in office and 4 days from home. Platform Engineer Experience Linux operating systems, Debian and RHEL/Centos Google Cloud Platform (GCP) or AWS Infrastructure as Code best practises (Terraform) Configuration Management - Ansible, Puppet, Packer Containerization - Docker & Kubernetes Knowledge of Continuous Integration processes - Jenkins and GitHub Scripting/programming languages (Python, Bash, Perl or Golang) Databases (primarily MySQL) DNs would also be beneficial (Fastly) We are not expecting the Platform Engineer to be an expert in everything above, just a strong basis knowledge and passion to learn more! You will be an enthusiastic Platform Engineer, a great communicator and have an inquisitive attitude. The successful Platform Engineer should have strong problem-solving abilities, organisational skills, and the ability to work as part of a team. We are interviewing currently so apply now for immediate consideration for the Platform Engineer position or contact George Harvey at ITSS Recruitment for further information.
React Developer (Software Engineer Programmer Developer React TypeScript Redux Saga Ag-Grid OpenFin Figma Fixed Income JavaScript Fixed Income Credit Rates Bonds ABS Agile AWS GCP Buy Side Asset Manager Investment Management Banking Financial Finance Front Office Trading Financial Services Front End Frontend Front End) required by our trading software client in London. You MUST have the following: Experience as a Senior/Lead React Developer/Software Engineer/Programmer Excellent JavaScript, TypeScript and React Redux Good Ag-Grid Financial markets/trading experience Excellent stakeholder interaction skills Agile The following is DESIRABLE, not essential: OpenFin or equivalent desktop interoperability tools Figma Role: React Developer (Software Engineer Programmer Developer React TypeScript Redux Saga Ag-Grid OpenFin Figma Fixed Income JavaScript Fixed Income Credit Rates Bonds ABS Agile AWS GCP Buy Side Asset Manager Investment Management Banking Financial Finance Front Office Trading Financial Services Front End Frontend Front End) required by our trading software client in London. You will be joining a very small, very high-performing team of a Back End developer and a product owner who are building a new tool for their trading technology suite. You will therefore be the sole and lead Front End developer for the product. As it gains momentum however, the team will grow and you will be assisted by a junior-mid level engineer. The tech stack is React, Ag-Grid, TypeScript, Redux, OpenFin and Figma. Experience with React, TypeScript, Redux and Ag-Grid is essential. OpenFin and Figma are only desirable. The role will have an element of design but this will mostly be the responsibility of the UX team. Likewise, there is a central UI engineering team that builds component libraries and structures that you will be able to use to accelerate delivery and scalability. As this is a small team, you will be comfortable as a sole Front End developer in a greenfield project setting. You will be a high-performer and excellent collaborator. Hours are 8:30am - 5.30pm and hybrid working means 2 days in the office. Salary: £110k - £140k + 30% Bonus + 10% Pension
Mar 21, 2025
Full time
React Developer (Software Engineer Programmer Developer React TypeScript Redux Saga Ag-Grid OpenFin Figma Fixed Income JavaScript Fixed Income Credit Rates Bonds ABS Agile AWS GCP Buy Side Asset Manager Investment Management Banking Financial Finance Front Office Trading Financial Services Front End Frontend Front End) required by our trading software client in London. You MUST have the following: Experience as a Senior/Lead React Developer/Software Engineer/Programmer Excellent JavaScript, TypeScript and React Redux Good Ag-Grid Financial markets/trading experience Excellent stakeholder interaction skills Agile The following is DESIRABLE, not essential: OpenFin or equivalent desktop interoperability tools Figma Role: React Developer (Software Engineer Programmer Developer React TypeScript Redux Saga Ag-Grid OpenFin Figma Fixed Income JavaScript Fixed Income Credit Rates Bonds ABS Agile AWS GCP Buy Side Asset Manager Investment Management Banking Financial Finance Front Office Trading Financial Services Front End Frontend Front End) required by our trading software client in London. You will be joining a very small, very high-performing team of a Back End developer and a product owner who are building a new tool for their trading technology suite. You will therefore be the sole and lead Front End developer for the product. As it gains momentum however, the team will grow and you will be assisted by a junior-mid level engineer. The tech stack is React, Ag-Grid, TypeScript, Redux, OpenFin and Figma. Experience with React, TypeScript, Redux and Ag-Grid is essential. OpenFin and Figma are only desirable. The role will have an element of design but this will mostly be the responsibility of the UX team. Likewise, there is a central UI engineering team that builds component libraries and structures that you will be able to use to accelerate delivery and scalability. As this is a small team, you will be comfortable as a sole Front End developer in a greenfield project setting. You will be a high-performer and excellent collaborator. Hours are 8:30am - 5.30pm and hybrid working means 2 days in the office. Salary: £110k - £140k + 30% Bonus + 10% Pension
CK Group are working with a long established and successful pharmaceutical company in Hertfordshire. They are about to transition from paper-based clinical study processes, to a fully electronic system and are looking for a permanent Clinical Computer Systems Manager to oversee that. This will be fully office based in Hertfordshire to start with, but can go down to three days a week in the office once settled in. RESPONSIBILITIES: As Clinical Computer Systems Manager you will collaborate closely with colleagues in Clinical, Regulatory, Quality and Systems to implement and optimise electronic clinical systems, ensuring compliance with GCP, MHRA, EMA and GDPR regulations. Key duties will include: Defining and executing a digital transformation roadmap for clinical systems. Leading the selection, validation and implementation of EDC, eTMF and CTMS to improve efficiency and support clinical and regulatory requirements. Working closely with the clinical team to define system requirements, workflows and individual clinical study needs. Leading system configuration, validation and User Acceptance Testing to ensure compliance with 21 CFR Part 11, GCP Data Governance and GDPR. Developing and managing clinical electronic system SOPs, work instructions and training materials. Ensuring data security, integrity and compliance across all clinical systems for the system lifecycle. QUALIFICATIONS: As Clinical Computer Systems Manager you will require: A relevant life science, computer science or similar degree. Extensive experience of managing electronic clinical trials system such as EDC, eTMF, CTMS etc. An in-depth knowledge of clinical trial processes, ICH-GCP, GDPR, ISO 14155:2020 and MHRA/EMA regulations. Experience of Computer System Validation and systems vendor selection. Excellent project management skills. The ability to train and support clinical teams during system transitions and throughout the electronic system lifecycle. BENEFITS: Competitive salary. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Mar 21, 2025
Full time
CK Group are working with a long established and successful pharmaceutical company in Hertfordshire. They are about to transition from paper-based clinical study processes, to a fully electronic system and are looking for a permanent Clinical Computer Systems Manager to oversee that. This will be fully office based in Hertfordshire to start with, but can go down to three days a week in the office once settled in. RESPONSIBILITIES: As Clinical Computer Systems Manager you will collaborate closely with colleagues in Clinical, Regulatory, Quality and Systems to implement and optimise electronic clinical systems, ensuring compliance with GCP, MHRA, EMA and GDPR regulations. Key duties will include: Defining and executing a digital transformation roadmap for clinical systems. Leading the selection, validation and implementation of EDC, eTMF and CTMS to improve efficiency and support clinical and regulatory requirements. Working closely with the clinical team to define system requirements, workflows and individual clinical study needs. Leading system configuration, validation and User Acceptance Testing to ensure compliance with 21 CFR Part 11, GCP Data Governance and GDPR. Developing and managing clinical electronic system SOPs, work instructions and training materials. Ensuring data security, integrity and compliance across all clinical systems for the system lifecycle. QUALIFICATIONS: As Clinical Computer Systems Manager you will require: A relevant life science, computer science or similar degree. Extensive experience of managing electronic clinical trials system such as EDC, eTMF, CTMS etc. An in-depth knowledge of clinical trial processes, ICH-GCP, GDPR, ISO 14155:2020 and MHRA/EMA regulations. Experience of Computer System Validation and systems vendor selection. Excellent project management skills. The ability to train and support clinical teams during system transitions and throughout the electronic system lifecycle. BENEFITS: Competitive salary. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services) required by our asset management client in London. You MUST have the following: Strong experience as a Python Developer/Software Engineer/Programmer Excellent Python Experience working in Front Office financial trading (eg. Fixed Income, equities, FX or commodities) Some Front End ability (Vue, React or Angular good but not necessary) Agile The following is DESIRABLE, not essential: AWS or GCP Buy-side Data tools such as Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio Fixed Income performance, risk or attribution TypeScript and Node Role: Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services Pandas Numpy Scipy) required by our asset management client in London. You will join a team of 4 that is responsible for an in-house built order tracking and communication platform. It will allow portfolio managers to communicate trade orders to investment analysts in a way that can be tracked and aligned with investment strategies and risk management. The role will have a Back End emphasis, which will be Python, AWS and PostgreSQL but you will also have some ability to contribute towards the React Front End. The project is at inception and the first demo has been approved by the business. It now has to be built out. There will be an excellent opportunity here to improve your knowledge of Fixed Income products and trading. They have a hybrid-working set up that requires the team to be in the office 1-2 times a week. The tech environment is very new and will soon likely include exposure to the following: Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio This is an environment that has been described as the only corporate environment with a start-up/fintech attitude towards technology. Hours are 9-5. Salary: £95k - £115k + 10% Bonus + 10% Pension
Mar 20, 2025
Full time
Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services) required by our asset management client in London. You MUST have the following: Strong experience as a Python Developer/Software Engineer/Programmer Excellent Python Experience working in Front Office financial trading (eg. Fixed Income, equities, FX or commodities) Some Front End ability (Vue, React or Angular good but not necessary) Agile The following is DESIRABLE, not essential: AWS or GCP Buy-side Data tools such as Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio Fixed Income performance, risk or attribution TypeScript and Node Role: Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services Pandas Numpy Scipy) required by our asset management client in London. You will join a team of 4 that is responsible for an in-house built order tracking and communication platform. It will allow portfolio managers to communicate trade orders to investment analysts in a way that can be tracked and aligned with investment strategies and risk management. The role will have a Back End emphasis, which will be Python, AWS and PostgreSQL but you will also have some ability to contribute towards the React Front End. The project is at inception and the first demo has been approved by the business. It now has to be built out. There will be an excellent opportunity here to improve your knowledge of Fixed Income products and trading. They have a hybrid-working set up that requires the team to be in the office 1-2 times a week. The tech environment is very new and will soon likely include exposure to the following: Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio This is an environment that has been described as the only corporate environment with a start-up/fintech attitude towards technology. Hours are 9-5. Salary: £95k - £115k + 10% Bonus + 10% Pension
Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services) required by our asset management client in London. You MUST have the following: Strong experience as a Python Developer/Software Engineer/Programmer Excellent Python Experience working in Front Office financial trading (eg. Fixed Income, equities, FX or commodities) Some Front End ability (Vue, React or Angular good but not necessary) Agile The following is DESIRABLE, not essential: AWS or GCP Buy-side Data tools such as Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio Fixed Income performance, risk or attribution TypeScript and Node Role: Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services Pandas Numpy Scipy) required by our asset management client in London. You will join a team of 4 that is responsible for an in-house built order tracking and communication platform. It will allow portfolio managers to communicate trade orders to investment analysts in a way that can be tracked and aligned with investment strategies and risk management. The role will have a Back End emphasis, which will be Python, AWS and PostgreSQL but you will also have some ability to contribute towards the React Front End. The project is at inception and the first demo has been approved by the business. It now has to be built out. There will be an excellent opportunity here to improve your knowledge of Fixed Income products and trading. They have a hybrid-working set up that requires the team to be in the office 1-2 times a week. The tech environment is very new and will soon likely include exposure to the following: Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio This is an environment that has been described as the only corporate environment with a start-up/fintech attitude towards technology. Hours are 9-5. Salary: £115k - £145k + 10% Bonus + 10% Pension
Mar 20, 2025
Full time
Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services) required by our asset management client in London. You MUST have the following: Strong experience as a Python Developer/Software Engineer/Programmer Excellent Python Experience working in Front Office financial trading (eg. Fixed Income, equities, FX or commodities) Some Front End ability (Vue, React or Angular good but not necessary) Agile The following is DESIRABLE, not essential: AWS or GCP Buy-side Data tools such as Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio Fixed Income performance, risk or attribution TypeScript and Node Role: Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services Pandas Numpy Scipy) required by our asset management client in London. You will join a team of 4 that is responsible for an in-house built order tracking and communication platform. It will allow portfolio managers to communicate trade orders to investment analysts in a way that can be tracked and aligned with investment strategies and risk management. The role will have a Back End emphasis, which will be Python, AWS and PostgreSQL but you will also have some ability to contribute towards the React Front End. The project is at inception and the first demo has been approved by the business. It now has to be built out. There will be an excellent opportunity here to improve your knowledge of Fixed Income products and trading. They have a hybrid-working set up that requires the team to be in the office 1-2 times a week. The tech environment is very new and will soon likely include exposure to the following: Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio This is an environment that has been described as the only corporate environment with a start-up/fintech attitude towards technology. Hours are 9-5. Salary: £115k - £145k + 10% Bonus + 10% Pension
Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services) required by our asset management client in London. You MUST have the following: Strong experience as a Python Developer/Software Engineer/Programmer Excellent Python Experience working in trading environments (Fixed Income, equities, commodities, FX etc) Some Front End ability (Vue, React or Angular good but not necessary) Agile The following is DESIRABLE, not essential: AWS or GCP Buy-side Data tools such as Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio Fixed Income performance, risk or attribution TypeScript and Node Role: Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services Pandas Numpy Scipy) required by our asset management client in London. You will join a team of 4 that is responsible for an in-house built order tracking and communication platform. It will allow portfolio managers to communicate trade orders to investment analysts in a way that can be tracked and aligned with investment strategies and risk management. The role will have a Back End emphasis, which will be Python, AWS and PostgreSQL but you will also have some ability to contribute towards the React Front End. The project is at inception and the first demo has been approved by the business. It now has to be built out. There will be an excellent opportunity here to improve your knowledge of Fixed Income products and trading. They have a hybrid-working set up that requires the team to be in the office 1-2 times a week. The tech environment is very new and will soon likely include exposure to the following: Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio This is an environment that has been described as the only corporate environment with a start-up/fintech attitude towards technology. Hours are 9-5. Salary: £115k - £145k + 10% Bonus + 10% Pension
Mar 20, 2025
Full time
Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services) required by our asset management client in London. You MUST have the following: Strong experience as a Python Developer/Software Engineer/Programmer Excellent Python Experience working in trading environments (Fixed Income, equities, commodities, FX etc) Some Front End ability (Vue, React or Angular good but not necessary) Agile The following is DESIRABLE, not essential: AWS or GCP Buy-side Data tools such as Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio Fixed Income performance, risk or attribution TypeScript and Node Role: Python Developer (Software Engineer Programmer Developer Python Fixed Income JavaScript Node Fixed Income Credit Rates Bonds ABS Vue Angular React Agile AWS GCP Buy Side Asset Manager Investment Management Performance Risk Attribution TypeScript Node Finance Front Office Trading Financial Services Pandas Numpy Scipy) required by our asset management client in London. You will join a team of 4 that is responsible for an in-house built order tracking and communication platform. It will allow portfolio managers to communicate trade orders to investment analysts in a way that can be tracked and aligned with investment strategies and risk management. The role will have a Back End emphasis, which will be Python, AWS and PostgreSQL but you will also have some ability to contribute towards the React Front End. The project is at inception and the first demo has been approved by the business. It now has to be built out. There will be an excellent opportunity here to improve your knowledge of Fixed Income products and trading. They have a hybrid-working set up that requires the team to be in the office 1-2 times a week. The tech environment is very new and will soon likely include exposure to the following: Glue, Athena, Airflow, Ignite, DBT, Arrow, Iceberg, Dremio This is an environment that has been described as the only corporate environment with a start-up/fintech attitude towards technology. Hours are 9-5. Salary: £115k - £145k + 10% Bonus + 10% Pension
Clinical Project Manager II Location: Oxford, Oxfordshire, United Kingdom Postcode: OX4 2LL Type of contract : Permanent Salary: 40,000 to 60,000 Per Annum Closing Date: Monday, April 14, 2025 Are you an experienced Clinical Project Manager or do you have experience with Clinical Trials? Are you looking for your next challenge within a growing organisation? About the Role As one of our dedicated Clinical Project Managers, you will be managing and delivering commercially sponsored investigational trials. Day to day your duties will include: Managing interactions between key project stakeholders for assigned clinical studies: Meeting Management: Conduct engaging and well-organised project meetings, both on and off-site, that spark collaboration and innovation, capturing all details. Contracts: Safeguard the critical contracts necessary for study success. Financials: Collaborate with our Finance team to steer the financial course of ongoing projects, overseeing monthly budgeting and forecasting. Timelines: Vigilantly track project progression, ensuring we stay on course with predefined timelines. Strategic Reporting: Craft insightful reports that align seamlessly with project milestones and deliverables. Stakeholder Communication: Provide seamless communication among stakeholders during the conduct of clinical trials. Compliance: Lead the way in sponsoring and adhering to ICH-GCP standards for Perspectum-sponsored trials, all while expertly managing vital trial documentation and delivering results with precision and timeliness. Demonstrate understanding of Perspectum products and services including how the Clinical Project Manager II role collaborates with internal departments. About You To be successful in this role you will have/be: Ability to problem solve over a complex range of tasks subject to competing contractual, financial, personnel and time constraints Excellent communication skills, both oral and written, and the ability to use these skills to execute project management duties Ability to manage bandwidth and assignments across a portfolio of projects identifying proactively when more support is needed Proven experience working with clinical trials and a strong understanding of the clinical trial process Above all you will be self-motivated and driven to achieve your personal and team objectives to support the wider business goals. About Perspectum All our benefits information can be found in the downloadable Benefits document under 'Information' on the right hand side of this screen. At Perspectum, we are committed to fostering diversity, equity, and inclusion. We prioritise hiring based on merit, skills, and qualifications, valuing individuals for their unique contributions while ensuring a culture that respects and celebrates differences. If you require any reasonable adjustments as part of your application process, please let our Talent Team know. REF-(phone number removed)
Mar 19, 2025
Full time
Clinical Project Manager II Location: Oxford, Oxfordshire, United Kingdom Postcode: OX4 2LL Type of contract : Permanent Salary: 40,000 to 60,000 Per Annum Closing Date: Monday, April 14, 2025 Are you an experienced Clinical Project Manager or do you have experience with Clinical Trials? Are you looking for your next challenge within a growing organisation? About the Role As one of our dedicated Clinical Project Managers, you will be managing and delivering commercially sponsored investigational trials. Day to day your duties will include: Managing interactions between key project stakeholders for assigned clinical studies: Meeting Management: Conduct engaging and well-organised project meetings, both on and off-site, that spark collaboration and innovation, capturing all details. Contracts: Safeguard the critical contracts necessary for study success. Financials: Collaborate with our Finance team to steer the financial course of ongoing projects, overseeing monthly budgeting and forecasting. Timelines: Vigilantly track project progression, ensuring we stay on course with predefined timelines. Strategic Reporting: Craft insightful reports that align seamlessly with project milestones and deliverables. Stakeholder Communication: Provide seamless communication among stakeholders during the conduct of clinical trials. Compliance: Lead the way in sponsoring and adhering to ICH-GCP standards for Perspectum-sponsored trials, all while expertly managing vital trial documentation and delivering results with precision and timeliness. Demonstrate understanding of Perspectum products and services including how the Clinical Project Manager II role collaborates with internal departments. About You To be successful in this role you will have/be: Ability to problem solve over a complex range of tasks subject to competing contractual, financial, personnel and time constraints Excellent communication skills, both oral and written, and the ability to use these skills to execute project management duties Ability to manage bandwidth and assignments across a portfolio of projects identifying proactively when more support is needed Proven experience working with clinical trials and a strong understanding of the clinical trial process Above all you will be self-motivated and driven to achieve your personal and team objectives to support the wider business goals. About Perspectum All our benefits information can be found in the downloadable Benefits document under 'Information' on the right hand side of this screen. At Perspectum, we are committed to fostering diversity, equity, and inclusion. We prioritise hiring based on merit, skills, and qualifications, valuing individuals for their unique contributions while ensuring a culture that respects and celebrates differences. If you require any reasonable adjustments as part of your application process, please let our Talent Team know. REF-(phone number removed)
CK Group are recruiting for a Clinical Project Manager, to join a leading provider of advanced analytics research and technology solutions to the life sciences industry, at their site based in Paddington, London, Basildon, and working from home, on a contract basis for 12 months. This role is a hybrid position. Rate : £30.08 per hour PAYE. Clinical Project Manager Role: Overseeing the budget for clinical trials and ensuring that resources are allocated appropriately. Including managing staff, equipment, and supplies, as well as monitoring expenses and identifying cost-saving measures. Recruiting, training, and supervising vendor/staff, including clinical research associates and data managers. Ensure that vendor/staff are properly trained on study protocols and that they follow GCP guidelines and other regulatory requirements. Ensuring the integrity and accuracy of clinical trial data by overseeing data management activities, including data collection, analysis, and reporting as well as ensuring that data is stored securely and in compliance with regulatory requirements. Developing and implementing quality control measures to ensure compliance with regulatory requirements and standards. Liaising with study CROs, principal investigators, and other stakeholders to provide regular updates on study progress and to address any issues or concerns that arise during the course of the study. Your Background : Knowledge of budgeting and tracking. Strong knowledge of safety and ethics. Ability to coordinate site management with research activities. Experience within outsourcing and contracts within the Pharmaceutical industry is preferred or at least demonstrable knowledge of contracts, bid meetings and negotiations. Minimum 5+ years of experience in clinical trial management. Detail-oriented, analytical, and able to work effectively in a team environment Company: Our client offers research services and technology solutions in the life sciences industry. With just under 100,000 employees, the company has operations in over 90 countries worldwide. Our client s ambitions involve optimising results of innovations using artificial intelligence. They believe in utilising data collected to the maximum rather than focussing on gathering lots of information: they use artificial intelligence to do this. Location: This role is a hybrid role, it is based at our client s site in Paddington, London and also Basildon. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Mar 19, 2025
Full time
CK Group are recruiting for a Clinical Project Manager, to join a leading provider of advanced analytics research and technology solutions to the life sciences industry, at their site based in Paddington, London, Basildon, and working from home, on a contract basis for 12 months. This role is a hybrid position. Rate : £30.08 per hour PAYE. Clinical Project Manager Role: Overseeing the budget for clinical trials and ensuring that resources are allocated appropriately. Including managing staff, equipment, and supplies, as well as monitoring expenses and identifying cost-saving measures. Recruiting, training, and supervising vendor/staff, including clinical research associates and data managers. Ensure that vendor/staff are properly trained on study protocols and that they follow GCP guidelines and other regulatory requirements. Ensuring the integrity and accuracy of clinical trial data by overseeing data management activities, including data collection, analysis, and reporting as well as ensuring that data is stored securely and in compliance with regulatory requirements. Developing and implementing quality control measures to ensure compliance with regulatory requirements and standards. Liaising with study CROs, principal investigators, and other stakeholders to provide regular updates on study progress and to address any issues or concerns that arise during the course of the study. Your Background : Knowledge of budgeting and tracking. Strong knowledge of safety and ethics. Ability to coordinate site management with research activities. Experience within outsourcing and contracts within the Pharmaceutical industry is preferred or at least demonstrable knowledge of contracts, bid meetings and negotiations. Minimum 5+ years of experience in clinical trial management. Detail-oriented, analytical, and able to work effectively in a team environment Company: Our client offers research services and technology solutions in the life sciences industry. With just under 100,000 employees, the company has operations in over 90 countries worldwide. Our client s ambitions involve optimising results of innovations using artificial intelligence. They believe in utilising data collected to the maximum rather than focussing on gathering lots of information: they use artificial intelligence to do this. Location: This role is a hybrid role, it is based at our client s site in Paddington, London and also Basildon. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
CK Group are working with a commercially successful, privately owned biotech company, who are developing radiolabelled compounds for Oncology imaging and treatment. They are soon to begin their first Phase I study, and are looking for a permanent Clinical Study Manager to support this. This will be a fully home-based role, in either the UK or Germany. RESPONSIBILITIES: As Clinical Study Manager you will be an integral part of the Clinical Operations team, project managing Phase I & II studies against agreed milestones Key duties will include: Leading the clinical study team and ensuring delivery of studies within agreed timelines and budgets. Maintaining high quality and effective monitoring function and productive site relationships through the respective CROs and other vendors to ensure effective delivery and oversight. Preparation of key study documents such as protocols, amendments, informed consents, study procedure manuals, eCRFs, analytical plans, and other study documents through discussion with internal and external partners. Contribution to and review of documents for IMPDs/IBs/Protocols/CTAs/INDs and relevant regulatory section submissions. Through external partners, manage the study budget, timelines, study conduct and close out including involvement in the management of clinical trial material, which includes accurately projecting enrolment to ensure continuity of supply. In conjunction with the quality function, coordinate audit strategy/plans to ensure all clinical trial activities meet quality requirements including GCP, ICH, TGA, MHRA, EU and FDA guidelines and regulations as appropriate. QUALIFICATIONS: As Clinical Study Manager you will require: A relevant life science BSc / MSc / PhD. Proven clinical operations experience gained with Phase I & II Oncology trials. Extensive, industry-based experience of working in a GCP environment. Experience of managing clinical trial supplies. Experience of the selection and management of CROs and other suppliers. Strong Project Management skills. BENEFITS: Salary up to £85.000. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Mar 19, 2025
Full time
CK Group are working with a commercially successful, privately owned biotech company, who are developing radiolabelled compounds for Oncology imaging and treatment. They are soon to begin their first Phase I study, and are looking for a permanent Clinical Study Manager to support this. This will be a fully home-based role, in either the UK or Germany. RESPONSIBILITIES: As Clinical Study Manager you will be an integral part of the Clinical Operations team, project managing Phase I & II studies against agreed milestones Key duties will include: Leading the clinical study team and ensuring delivery of studies within agreed timelines and budgets. Maintaining high quality and effective monitoring function and productive site relationships through the respective CROs and other vendors to ensure effective delivery and oversight. Preparation of key study documents such as protocols, amendments, informed consents, study procedure manuals, eCRFs, analytical plans, and other study documents through discussion with internal and external partners. Contribution to and review of documents for IMPDs/IBs/Protocols/CTAs/INDs and relevant regulatory section submissions. Through external partners, manage the study budget, timelines, study conduct and close out including involvement in the management of clinical trial material, which includes accurately projecting enrolment to ensure continuity of supply. In conjunction with the quality function, coordinate audit strategy/plans to ensure all clinical trial activities meet quality requirements including GCP, ICH, TGA, MHRA, EU and FDA guidelines and regulations as appropriate. QUALIFICATIONS: As Clinical Study Manager you will require: A relevant life science BSc / MSc / PhD. Proven clinical operations experience gained with Phase I & II Oncology trials. Extensive, industry-based experience of working in a GCP environment. Experience of managing clinical trial supplies. Experience of the selection and management of CROs and other suppliers. Strong Project Management skills. BENEFITS: Salary up to £85.000. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Senior PHP Engineer Remote working with offices based in Bournemouth, Dorset. Salary up to 60,000 plus bonus and benefits OOP, PHP, LAMP, MVC Laravel, RESTful APIs, GCP There are companies that tick over, there are teams that plod, there are products that have aged and there are managers that think this is fine and dandy! Not us and not this company. We are looking for a talented Senior PHP Developer to join one of the UK's fastest growing and most exciting digital companies. Build new products, engineer new solutions, create systems and platforms that enable people all over the world to connect through a single digital marketplace. This is just the start. About You: You are an experienced Senior PHP Developer with strong back end PHP / LAMP stack experience, sound knowledge of OOP, design principles and building quality, robust and reusable solutions. You like people and working with them day to day! You enjoy team collaboration when required and knuckling down to write quality, testable, reusable code when that's the task at hand. The Team: You will join a diverse team of software & web engineers working on a range of digital solutions delivered to 120+ countries worldwide. The solutions are digital retail, ecommerce and web services and include the development & design of systems, platforms, website and much more. Successful developers in this team demonstrate passion and enthusiasm and a willingness to contribute to team goals, help others and to keep improving and evolving their own skills. The tech stack: OOP PHP8+ MySQL LAMP MVC frameworks including Laravel GIT/Source Control HTML, CSS JavaScript GCP This position provides the successful candidate with the exposure to the very latest in web technology release as well as the opportunity to work on multiple projects. Apply now - Please send your CV or an introduction email to (url removed). Find me on LinkedIN, Twitter and through the Spectrum IT Recruitment website. Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
Mar 18, 2025
Full time
Senior PHP Engineer Remote working with offices based in Bournemouth, Dorset. Salary up to 60,000 plus bonus and benefits OOP, PHP, LAMP, MVC Laravel, RESTful APIs, GCP There are companies that tick over, there are teams that plod, there are products that have aged and there are managers that think this is fine and dandy! Not us and not this company. We are looking for a talented Senior PHP Developer to join one of the UK's fastest growing and most exciting digital companies. Build new products, engineer new solutions, create systems and platforms that enable people all over the world to connect through a single digital marketplace. This is just the start. About You: You are an experienced Senior PHP Developer with strong back end PHP / LAMP stack experience, sound knowledge of OOP, design principles and building quality, robust and reusable solutions. You like people and working with them day to day! You enjoy team collaboration when required and knuckling down to write quality, testable, reusable code when that's the task at hand. The Team: You will join a diverse team of software & web engineers working on a range of digital solutions delivered to 120+ countries worldwide. The solutions are digital retail, ecommerce and web services and include the development & design of systems, platforms, website and much more. Successful developers in this team demonstrate passion and enthusiasm and a willingness to contribute to team goals, help others and to keep improving and evolving their own skills. The tech stack: OOP PHP8+ MySQL LAMP MVC frameworks including Laravel GIT/Source Control HTML, CSS JavaScript GCP This position provides the successful candidate with the exposure to the very latest in web technology release as well as the opportunity to work on multiple projects. Apply now - Please send your CV or an introduction email to (url removed). Find me on LinkedIN, Twitter and through the Spectrum IT Recruitment website. Spectrum IT Recruitment (South) Limited is acting as an Employment Agency in relation to this vacancy.
Locations : Atlanta London Who We Are Boston Consulting Group partners with leaders in business and society to tackle their most important challenges and capture their greatest opportunities. BCG was the pioneer in business strategy when it was founded in 1963. Today, we help clients with total transformation-inspiring complex change, enabling organizations to grow, building competitive advantage, and driving bottom-line impact. To succeed, organizations must blend digital and human capabilities. Our diverse, global teams bring deep industry and functional expertise and a range of perspectives to spark change. BCG delivers solutions through leading-edge management consulting along with technology and design, corporate and digital ventures-and business purpose. We work in a uniquely collaborative model across the firm and throughout all levels of the client organization, generating results that allow our clients to thrive. What You'll Do This role focuses on designing, implementing, and tracking cloud security enhancements with a specialization in Secrets Management across multi-cloud and SaaS environments. You will influence engineering decisions to drive secure and successful business outcomes while collaborating with internal teams to protect enterprise information. Key responsibilities include defining and implementing identity, access, and security requirements; planning, testing, and supporting secure systems; and serving as a Subject Matter Expert on IT projects. Additionally, you will develop and maintain security standards, policies, and procedures, while mentoring team members to foster a strong security culture. This position requires a strategic and hands-on approach to strengthen BCG's cloud security posture. YOU'RE GOOD AT Interacting with stakeholders and possessing the ability to influence direction, articulate risks and advocate for solutions and roadmaps. Managing backlog and roadmap of secrets management items to be completed. Managing end to end delivery of projects with hands on involvement in the development and configuration of products around secrets management and machine authentication. Determining requirements by evaluating business strategies and requirements, implementing information security standards, conducting system and vulnerability analyses and risk assessments, recommending secure architecture aligned to business architecture, and identifying/driving remediation of integration issues. Providing expert knowledge of solution/application architecture for identity related capabilities as well as methodologies in the software development life cycle. Maintaining security data and identity principles by ensuring compliance to standards, policies, regulatory requirements, and good industry practices are achieved. Self-managing progress and status of tasks and deliverables on projects and escalating issues and risks timely. Completing market assessments on vendor products, packages, and services; guiding tests and implementation of products solving enterprise information security requirements. Suggesting and implementing alternative mitigations/compensating controls to allow for business to continue while protecting BCG's assets. Partnering with cross functional teams to ensure compliance to industry and company standards including ISO 27001, SOC2, NIST, GDPR, and DPO standards. Updating job knowledge by tracking and understanding emerging practices and standards; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. Vendor escalations and Major Incident Management support for business-critical services. Able to provide L3 operational support for Secrets Management tooling and oversight of L1/L2 ops issues. Create and track health, security and adoption metrics. What You'll Bring Must Haves: Ability to drive adoption of secrets management best practices, primarily using HashiCorp Vault 3+ years' experience of secrets management through large scale implementations distributed globally Experience managing cloud native secrets management solutions such as Azure Key Vault, Google Secrets Manager and AWS Secrets Manager. Experience with Cloud Security Posture Management (CSPM) across the cloud platforms including AWS, Azure, and GCP Tier 3 support experience for service outage and mission-critical application support Experience with app registrations and service principals in Azure AD Experience documenting complex architectures Experience with GitHub, (or similar tools including Chef or Puppet), Continuous Integration/Continuous Deployment (CI/CD) Knowledge and experience with automating solutions using one or more languages (i.e., Python, PowerShell, Terraform, or similar) Nice Haves: Bachelor's degree (or equivalent related experience) 7+ years' experience working with AWS, GCP, Azure, or Alibaba cloud Understanding of API concepts and RESTful services Understanding of cloud security, zero trust, risk-based authentication, and multi-factor authentication (MFA) solutions Hands-on/direct experience integrating web, single-page, native applications through API endpoints, API services for machine-to-machine authentication Related certifications (e.g. Security Plus, CISSP, CCSP, ITIL Foundations, CE+, etc) Experience working in Agile, knowledge of Jira, Jira Align, Miro, and related tools and principals Experience as a change management practitioner using industry best practices and ServiceNow tooling and workflows Boston Consulting Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity / expression, national origin, disability, protected veteran status, or any other characteristic protected under national, provincial, or local law, where applicable, and those with criminal histories will be considered in a manner consistent with applicable state and local laws. BCG is an E - Verify Employer. Click here for more information on E-Verify.
Mar 18, 2025
Full time
Locations : Atlanta London Who We Are Boston Consulting Group partners with leaders in business and society to tackle their most important challenges and capture their greatest opportunities. BCG was the pioneer in business strategy when it was founded in 1963. Today, we help clients with total transformation-inspiring complex change, enabling organizations to grow, building competitive advantage, and driving bottom-line impact. To succeed, organizations must blend digital and human capabilities. Our diverse, global teams bring deep industry and functional expertise and a range of perspectives to spark change. BCG delivers solutions through leading-edge management consulting along with technology and design, corporate and digital ventures-and business purpose. We work in a uniquely collaborative model across the firm and throughout all levels of the client organization, generating results that allow our clients to thrive. What You'll Do This role focuses on designing, implementing, and tracking cloud security enhancements with a specialization in Secrets Management across multi-cloud and SaaS environments. You will influence engineering decisions to drive secure and successful business outcomes while collaborating with internal teams to protect enterprise information. Key responsibilities include defining and implementing identity, access, and security requirements; planning, testing, and supporting secure systems; and serving as a Subject Matter Expert on IT projects. Additionally, you will develop and maintain security standards, policies, and procedures, while mentoring team members to foster a strong security culture. This position requires a strategic and hands-on approach to strengthen BCG's cloud security posture. YOU'RE GOOD AT Interacting with stakeholders and possessing the ability to influence direction, articulate risks and advocate for solutions and roadmaps. Managing backlog and roadmap of secrets management items to be completed. Managing end to end delivery of projects with hands on involvement in the development and configuration of products around secrets management and machine authentication. Determining requirements by evaluating business strategies and requirements, implementing information security standards, conducting system and vulnerability analyses and risk assessments, recommending secure architecture aligned to business architecture, and identifying/driving remediation of integration issues. Providing expert knowledge of solution/application architecture for identity related capabilities as well as methodologies in the software development life cycle. Maintaining security data and identity principles by ensuring compliance to standards, policies, regulatory requirements, and good industry practices are achieved. Self-managing progress and status of tasks and deliverables on projects and escalating issues and risks timely. Completing market assessments on vendor products, packages, and services; guiding tests and implementation of products solving enterprise information security requirements. Suggesting and implementing alternative mitigations/compensating controls to allow for business to continue while protecting BCG's assets. Partnering with cross functional teams to ensure compliance to industry and company standards including ISO 27001, SOC2, NIST, GDPR, and DPO standards. Updating job knowledge by tracking and understanding emerging practices and standards; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. Vendor escalations and Major Incident Management support for business-critical services. Able to provide L3 operational support for Secrets Management tooling and oversight of L1/L2 ops issues. Create and track health, security and adoption metrics. What You'll Bring Must Haves: Ability to drive adoption of secrets management best practices, primarily using HashiCorp Vault 3+ years' experience of secrets management through large scale implementations distributed globally Experience managing cloud native secrets management solutions such as Azure Key Vault, Google Secrets Manager and AWS Secrets Manager. Experience with Cloud Security Posture Management (CSPM) across the cloud platforms including AWS, Azure, and GCP Tier 3 support experience for service outage and mission-critical application support Experience with app registrations and service principals in Azure AD Experience documenting complex architectures Experience with GitHub, (or similar tools including Chef or Puppet), Continuous Integration/Continuous Deployment (CI/CD) Knowledge and experience with automating solutions using one or more languages (i.e., Python, PowerShell, Terraform, or similar) Nice Haves: Bachelor's degree (or equivalent related experience) 7+ years' experience working with AWS, GCP, Azure, or Alibaba cloud Understanding of API concepts and RESTful services Understanding of cloud security, zero trust, risk-based authentication, and multi-factor authentication (MFA) solutions Hands-on/direct experience integrating web, single-page, native applications through API endpoints, API services for machine-to-machine authentication Related certifications (e.g. Security Plus, CISSP, CCSP, ITIL Foundations, CE+, etc) Experience working in Agile, knowledge of Jira, Jira Align, Miro, and related tools and principals Experience as a change management practitioner using industry best practices and ServiceNow tooling and workflows Boston Consulting Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity / expression, national origin, disability, protected veteran status, or any other characteristic protected under national, provincial, or local law, where applicable, and those with criminal histories will be considered in a manner consistent with applicable state and local laws. BCG is an E - Verify Employer. Click here for more information on E-Verify.
Locations : Atlanta London Who We Are Boston Consulting Group partners with leaders in business and society to tackle their most important challenges and capture their greatest opportunities. BCG was the pioneer in business strategy when it was founded in 1963. Today, we help clients with total transformation-inspiring complex change, enabling organizations to grow, building competitive advantage, and driving bottom-line impact. To succeed, organizations must blend digital and human capabilities. Our diverse, global teams bring deep industry and functional expertise and a range of perspectives to spark change. BCG delivers solutions through leading-edge management consulting along with technology and design, corporate and digital ventures-and business purpose. We work in a uniquely collaborative model across the firm and throughout all levels of the client organization, generating results that allow our clients to thrive. What You'll Do This role focuses on designing, implementing, and tracking cloud security enhancements with a specialization in Secrets Management across multi-cloud and SaaS environments. You will influence engineering decisions to drive secure and successful business outcomes while collaborating with internal teams to protect enterprise information. Key responsibilities include defining and implementing identity, access, and security requirements; planning, testing, and supporting secure systems; and serving as a Subject Matter Expert on IT projects. Additionally, you will develop and maintain security standards, policies, and procedures, while mentoring team members to foster a strong security culture. This position requires a strategic and hands-on approach to strengthen BCG's cloud security posture. YOU'RE GOOD AT Interacting with stakeholders and possessing the ability to influence direction, articulate risks and advocate for solutions and roadmaps. Managing backlog and roadmap of secrets management items to be completed. Managing end to end delivery of projects with hands on involvement in the development and configuration of products around secrets management and machine authentication. Determining requirements by evaluating business strategies and requirements, implementing information security standards, conducting system and vulnerability analyses and risk assessments, recommending secure architecture aligned to business architecture, and identifying/driving remediation of integration issues. Providing expert knowledge of solution/application architecture for identity related capabilities as well as methodologies in the software development life cycle. Maintaining security data and identity principles by ensuring compliance to standards, policies, regulatory requirements, and good industry practices are achieved. Self-managing progress and status of tasks and deliverables on projects and escalating issues and risks timely. Completing market assessments on vendor products, packages, and services; guiding tests and implementation of products solving enterprise information security requirements. Suggesting and implementing alternative mitigations/compensating controls to allow for business to continue while protecting BCG's assets. Partnering with cross functional teams to ensure compliance to industry and company standards including ISO 27001, SOC2, NIST, GDPR, and DPO standards. Updating job knowledge by tracking and understanding emerging practices and standards; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. Vendor escalations and Major Incident Management support for business-critical services. Able to provide L3 operational support for Secrets Management tooling and oversight of L1/L2 ops issues. Create and track health, security and adoption metrics. What You'll Bring Must Haves: Ability to drive adoption of secrets management best practices, primarily using HashiCorp Vault 3+ years' experience of secrets management through large scale implementations distributed globally Experience managing cloud native secrets management solutions such as Azure Key Vault, Google Secrets Manager and AWS Secrets Manager. Experience with Cloud Security Posture Management (CSPM) across the cloud platforms including AWS, Azure, and GCP Tier 3 support experience for service outage and mission-critical application support Experience with app registrations and service principals in Azure AD Experience documenting complex architectures Experience with GitHub, (or similar tools including Chef or Puppet), Continuous Integration/Continuous Deployment (CI/CD) Knowledge and experience with automating solutions using one or more languages (i.e., Python, PowerShell, Terraform, or similar) Nice Haves: Bachelor's degree (or equivalent related experience) 7+ years' experience working with AWS, GCP, Azure, or Alibaba cloud Understanding of API concepts and RESTful services Understanding of cloud security, zero trust, risk-based authentication, and multi-factor authentication (MFA) solutions Hands-on/direct experience integrating web, single-page, native applications through API endpoints, API services for machine-to-machine authentication Related certifications (e.g. Security Plus, CISSP, CCSP, ITIL Foundations, CE+, etc) Experience working in Agile, knowledge of Jira, Jira Align, Miro, and related tools and principals Experience as a change management practitioner using industry best practices and ServiceNow tooling and workflows Boston Consulting Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity / expression, national origin, disability, protected veteran status, or any other characteristic protected under national, provincial, or local law, where applicable, and those with criminal histories will be considered in a manner consistent with applicable state and local laws. BCG is an E - Verify Employer. Click here for more information on E-Verify.
Mar 18, 2025
Full time
Locations : Atlanta London Who We Are Boston Consulting Group partners with leaders in business and society to tackle their most important challenges and capture their greatest opportunities. BCG was the pioneer in business strategy when it was founded in 1963. Today, we help clients with total transformation-inspiring complex change, enabling organizations to grow, building competitive advantage, and driving bottom-line impact. To succeed, organizations must blend digital and human capabilities. Our diverse, global teams bring deep industry and functional expertise and a range of perspectives to spark change. BCG delivers solutions through leading-edge management consulting along with technology and design, corporate and digital ventures-and business purpose. We work in a uniquely collaborative model across the firm and throughout all levels of the client organization, generating results that allow our clients to thrive. What You'll Do This role focuses on designing, implementing, and tracking cloud security enhancements with a specialization in Secrets Management across multi-cloud and SaaS environments. You will influence engineering decisions to drive secure and successful business outcomes while collaborating with internal teams to protect enterprise information. Key responsibilities include defining and implementing identity, access, and security requirements; planning, testing, and supporting secure systems; and serving as a Subject Matter Expert on IT projects. Additionally, you will develop and maintain security standards, policies, and procedures, while mentoring team members to foster a strong security culture. This position requires a strategic and hands-on approach to strengthen BCG's cloud security posture. YOU'RE GOOD AT Interacting with stakeholders and possessing the ability to influence direction, articulate risks and advocate for solutions and roadmaps. Managing backlog and roadmap of secrets management items to be completed. Managing end to end delivery of projects with hands on involvement in the development and configuration of products around secrets management and machine authentication. Determining requirements by evaluating business strategies and requirements, implementing information security standards, conducting system and vulnerability analyses and risk assessments, recommending secure architecture aligned to business architecture, and identifying/driving remediation of integration issues. Providing expert knowledge of solution/application architecture for identity related capabilities as well as methodologies in the software development life cycle. Maintaining security data and identity principles by ensuring compliance to standards, policies, regulatory requirements, and good industry practices are achieved. Self-managing progress and status of tasks and deliverables on projects and escalating issues and risks timely. Completing market assessments on vendor products, packages, and services; guiding tests and implementation of products solving enterprise information security requirements. Suggesting and implementing alternative mitigations/compensating controls to allow for business to continue while protecting BCG's assets. Partnering with cross functional teams to ensure compliance to industry and company standards including ISO 27001, SOC2, NIST, GDPR, and DPO standards. Updating job knowledge by tracking and understanding emerging practices and standards; participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. Vendor escalations and Major Incident Management support for business-critical services. Able to provide L3 operational support for Secrets Management tooling and oversight of L1/L2 ops issues. Create and track health, security and adoption metrics. What You'll Bring Must Haves: Ability to drive adoption of secrets management best practices, primarily using HashiCorp Vault 3+ years' experience of secrets management through large scale implementations distributed globally Experience managing cloud native secrets management solutions such as Azure Key Vault, Google Secrets Manager and AWS Secrets Manager. Experience with Cloud Security Posture Management (CSPM) across the cloud platforms including AWS, Azure, and GCP Tier 3 support experience for service outage and mission-critical application support Experience with app registrations and service principals in Azure AD Experience documenting complex architectures Experience with GitHub, (or similar tools including Chef or Puppet), Continuous Integration/Continuous Deployment (CI/CD) Knowledge and experience with automating solutions using one or more languages (i.e., Python, PowerShell, Terraform, or similar) Nice Haves: Bachelor's degree (or equivalent related experience) 7+ years' experience working with AWS, GCP, Azure, or Alibaba cloud Understanding of API concepts and RESTful services Understanding of cloud security, zero trust, risk-based authentication, and multi-factor authentication (MFA) solutions Hands-on/direct experience integrating web, single-page, native applications through API endpoints, API services for machine-to-machine authentication Related certifications (e.g. Security Plus, CISSP, CCSP, ITIL Foundations, CE+, etc) Experience working in Agile, knowledge of Jira, Jira Align, Miro, and related tools and principals Experience as a change management practitioner using industry best practices and ServiceNow tooling and workflows Boston Consulting Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity / expression, national origin, disability, protected veteran status, or any other characteristic protected under national, provincial, or local law, where applicable, and those with criminal histories will be considered in a manner consistent with applicable state and local laws. BCG is an E - Verify Employer. Click here for more information on E-Verify.
CK Group are working with a commercially successful, privately owned biotech company, who are developing radiolabelled compounds for Oncology imaging and treatment. They are soon to begin their first Phase I study, and are looking for a permanent Clinical Study Manager to support this. This will be a fully home-based role, in either the UK or Germany. RESPONSIBILITIES: As Clinical Study Manager you will be an integral part of the Clinical Operations team, project managing Phase I & II studies against agreed milestones Key duties will include: Leading the clinical study team and ensuring delivery of studies within agreed timelines and budgets. Maintaining high quality and effective monitoring function and productive site relationships through the respective CROs and other vendors to ensure effective delivery and oversight. Preparation of key study documents such as protocols, amendments, informed consents, study procedure manuals, eCRFs, analytical plans, and other study documents through discussion with internal and external partners. Contribution to and review of documents for IMPDs/IBs/Protocols/CTAs/INDs and relevant regulatory section submissions. Through external partners, manage the study budget, timelines, study conduct and close out including involvement in the management of clinical trial material, which includes accurately projecting enrolment to ensure continuity of supply. In conjunction with the quality function, coordinate audit strategy/plans to ensure all clinical trial activities meet quality requirements including GCP, ICH, TGA, MHRA, EU and FDA guidelines and regulations as appropriate. QUALIFICATIONS: As Clinical Study Manager you will require: A relevant life science BSc / MSc / PhD. Proven clinical operations experience gained with Phase I & II Oncology trials. Extensive, industry-based experience of working in a GCP environment. Experience of managing clinical trial supplies. Experience of the selection and management of CROs and other suppliers. Strong Project Management skills. BENEFITS: Salary up to 85.000. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Mar 17, 2025
Full time
CK Group are working with a commercially successful, privately owned biotech company, who are developing radiolabelled compounds for Oncology imaging and treatment. They are soon to begin their first Phase I study, and are looking for a permanent Clinical Study Manager to support this. This will be a fully home-based role, in either the UK or Germany. RESPONSIBILITIES: As Clinical Study Manager you will be an integral part of the Clinical Operations team, project managing Phase I & II studies against agreed milestones Key duties will include: Leading the clinical study team and ensuring delivery of studies within agreed timelines and budgets. Maintaining high quality and effective monitoring function and productive site relationships through the respective CROs and other vendors to ensure effective delivery and oversight. Preparation of key study documents such as protocols, amendments, informed consents, study procedure manuals, eCRFs, analytical plans, and other study documents through discussion with internal and external partners. Contribution to and review of documents for IMPDs/IBs/Protocols/CTAs/INDs and relevant regulatory section submissions. Through external partners, manage the study budget, timelines, study conduct and close out including involvement in the management of clinical trial material, which includes accurately projecting enrolment to ensure continuity of supply. In conjunction with the quality function, coordinate audit strategy/plans to ensure all clinical trial activities meet quality requirements including GCP, ICH, TGA, MHRA, EU and FDA guidelines and regulations as appropriate. QUALIFICATIONS: As Clinical Study Manager you will require: A relevant life science BSc / MSc / PhD. Proven clinical operations experience gained with Phase I & II Oncology trials. Extensive, industry-based experience of working in a GCP environment. Experience of managing clinical trial supplies. Experience of the selection and management of CROs and other suppliers. Strong Project Management skills. BENEFITS: Salary up to 85.000. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Vacancy Name Principal Developer Vacancy No VN086 Location Portsmouth Employment Type Permanent Duration Type of Role Full-time If Rotating Shifts, please detail Job Advert We are looking to recruit a Principal Developer to join the team! We are united by passion in everything we do and driven by our winning teams who value the unique strengths we each bring. This is your opportunity to join a team who are not afraid to pursue ambitious goals and will support you to achieve your personal best. Whether you're a beginner or an expert, a sports enthusiast, or an excel expert, a people manager or an analyst, we have a place for you! There's a place for everyone in our team! You won't just be joining the WiggleCRC family, we're part of something bigger. We are now proud members of the Signa Sports United family! What's in it for you - The benefits If working alongside some for the most creative and innovative people isn't enough, we also offer you: Excellent career progression opportunities 25 days annual leave 5% pension contribution Staff discount Flexible working hours Healthcare plan Company Bonus Company sporting events, smart casual dress code, and brilliant company culture. What will you be doing? You will be responsible for the technical implementation strategy of our software projects. We are in the process of modernising its ecommerce platform and you will play a lead role in this project and on our future roadmap. Key Responsibilities: Leading the technical implementation of our strategy Building a technical talent pool. Helping to identify skills gaps and recruiting to fill those. Building relationships with delivery partners, ensuring quality and adherence to technical strategy. Supporting technical decision making, especially to facilitate delivery of future roadmap. Working closely with architects, product owners, business analysts to ensure delivery is feasible. Act as an SME for development decisions. Help to drive decisions on technology. Understand the impact those decisions will have to ensure the correct options are chosen. Ensuring the architecture of applications allows for flexibility and scalability. Make decisions that create reusable components. Mentoring other team members to ensure they're able to deliver software of the required quality. Line management of team members (monthly 1-1, 6-month review and goal setting) Drive best practices within the development team, including agile methodologies, automated testing, continuous deployment. Experience: Industry experience as a software developer Experience as a technical lead. You've been the person your colleagues come to when they need to understand the technical details Experience with multiple languages. We use Javascript, C# so knowledge of those would be an advantage, but there might be opportunities we're missing for others. Experience building modern websites. You know the pros and cons of react or angular. You're opinionated on SPAs and MFEs. Experience with testing frameworks. You know when to use TDD, BDD, you know the value of code coverage. Experience with REST, GraphQL and other communication protocols. You know when to keep it simple and when to push the boundaries. Experience with containerisation, cloud hosting. We use GCP and Azure. You like to use the right tool for the job, you don't reinvent the wheel, and you're confident in learning new technology. You understand the benefits of IAC. Experience with CI tooling. You believe your tools should make your life easier and to help prevent accidents. Being diverse and inclusive are key to our company values. You can find out more about the actions we're taking to support diversity on the Wiggle and Chain Reactions careers page on our websites.
Sep 24, 2022
Full time
Vacancy Name Principal Developer Vacancy No VN086 Location Portsmouth Employment Type Permanent Duration Type of Role Full-time If Rotating Shifts, please detail Job Advert We are looking to recruit a Principal Developer to join the team! We are united by passion in everything we do and driven by our winning teams who value the unique strengths we each bring. This is your opportunity to join a team who are not afraid to pursue ambitious goals and will support you to achieve your personal best. Whether you're a beginner or an expert, a sports enthusiast, or an excel expert, a people manager or an analyst, we have a place for you! There's a place for everyone in our team! You won't just be joining the WiggleCRC family, we're part of something bigger. We are now proud members of the Signa Sports United family! What's in it for you - The benefits If working alongside some for the most creative and innovative people isn't enough, we also offer you: Excellent career progression opportunities 25 days annual leave 5% pension contribution Staff discount Flexible working hours Healthcare plan Company Bonus Company sporting events, smart casual dress code, and brilliant company culture. What will you be doing? You will be responsible for the technical implementation strategy of our software projects. We are in the process of modernising its ecommerce platform and you will play a lead role in this project and on our future roadmap. Key Responsibilities: Leading the technical implementation of our strategy Building a technical talent pool. Helping to identify skills gaps and recruiting to fill those. Building relationships with delivery partners, ensuring quality and adherence to technical strategy. Supporting technical decision making, especially to facilitate delivery of future roadmap. Working closely with architects, product owners, business analysts to ensure delivery is feasible. Act as an SME for development decisions. Help to drive decisions on technology. Understand the impact those decisions will have to ensure the correct options are chosen. Ensuring the architecture of applications allows for flexibility and scalability. Make decisions that create reusable components. Mentoring other team members to ensure they're able to deliver software of the required quality. Line management of team members (monthly 1-1, 6-month review and goal setting) Drive best practices within the development team, including agile methodologies, automated testing, continuous deployment. Experience: Industry experience as a software developer Experience as a technical lead. You've been the person your colleagues come to when they need to understand the technical details Experience with multiple languages. We use Javascript, C# so knowledge of those would be an advantage, but there might be opportunities we're missing for others. Experience building modern websites. You know the pros and cons of react or angular. You're opinionated on SPAs and MFEs. Experience with testing frameworks. You know when to use TDD, BDD, you know the value of code coverage. Experience with REST, GraphQL and other communication protocols. You know when to keep it simple and when to push the boundaries. Experience with containerisation, cloud hosting. We use GCP and Azure. You like to use the right tool for the job, you don't reinvent the wheel, and you're confident in learning new technology. You understand the benefits of IAC. Experience with CI tooling. You believe your tools should make your life easier and to help prevent accidents. Being diverse and inclusive are key to our company values. You can find out more about the actions we're taking to support diversity on the Wiggle and Chain Reactions careers page on our websites.
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It Uniquely Yours. You work with business and IT stakeholders to support a future-state vision in terms of requirements, principles and models in a specific technology, process or function. How you will contribute Leads business process redesign, planning, and identifying touch points in multi-cloud implementations between systems to improve the process. Develops strong relationships with business by building trust, rapport and positive working relationships with key sponsors, stakeholders, and team members. Remain current with leading edge industry and technology drivers and innovations including the MuleSoft ,Talend and other integration products. Manage discussions with various levels of customer's business stakeholders Identify and help develop services offerings or provide technical guidance and support for MuleSoft & Talend Integration implementations Liaise with MuleSoft & Talend to support client implementations. Develop a product mindset and drive global template development model for global implementation. Validates solution components, leads technical guidance and provides guidance to the project manager for key issues/risks to the project Work with internal teams and business stakeholders to create prototypes, proof of concepts, etc. Lead and mentor other Integration Architects in the team. Create and own user overall Integration & Data Architecture for Integration initiatives support the Solution Architect from the Salesforce Hub(CoE). What you will bring A desire to drive your future and accelerate your career. You will bring experience and knowledge in: 10+ years CRM experience with a minimum of 5 years on the MuleSoft, Talend or any leading Integration platforms Expert & Hands On level understanding of the Integration product suite, including experience in integrating with Salesforce, SAP, GCP or AWS. Open to expand and explore Consumer Goods Domain. Experience in Consumer Goods domain will be an added advantage. Experience in being go to person for technical challenges to design and prioritise business requirements and required Capabilities. Ability to ask hard questions during sessions and suggest best practices and efficient ways of implementing business processes Proven ability to design and optimise business processes and to integrate business processes across disparate systems. Extensive experience in Integrating using MuleSoft/Talend or Other leading platforms with other Enterprise applications like Salesforce, SAP, GCP, AWS, etc with REST/SOAP APIs and Async processes. Ability to demonstrate concepts visually and in writing as the situation demands to guide stakeholders in thinking through all aspects of the ask Excellent analytical skills and the ability to develop processes and methodologies. Detail-oriented individual with the ability to rapidly learn and take advantage of new concepts, business models, and technologies. Strong background in leading large web-based systems, or complete software product lifecycle exposure Active MuleSoft certifications or ability to achieve relevant certifications upon hire Active Talend certification will be an added advantage. More about this role Work schedule: 100% No Relocation support available Business Unit Summary At Mondelēz International, our purpose is to empower people to snack right by offering the right snack, for the right moment, made the right way. That means delivering a broad range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about. We have a rich portfolio of strong brands globally and locally including many household names such as Oreo , belVita and LU biscuits; Cadbury Dairy Milk , Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the top position globally in biscuits, chocolate and candy and the second top position in gum. Our 80,000 makers and bakers are located in more than 80 countries and we sell our products in over 150 countries around the world. Our people are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen-and happen fast. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Regular Technology Architecture Technology & Digital
Sep 24, 2022
Full time
Job Description Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It Uniquely Yours. You work with business and IT stakeholders to support a future-state vision in terms of requirements, principles and models in a specific technology, process or function. How you will contribute Leads business process redesign, planning, and identifying touch points in multi-cloud implementations between systems to improve the process. Develops strong relationships with business by building trust, rapport and positive working relationships with key sponsors, stakeholders, and team members. Remain current with leading edge industry and technology drivers and innovations including the MuleSoft ,Talend and other integration products. Manage discussions with various levels of customer's business stakeholders Identify and help develop services offerings or provide technical guidance and support for MuleSoft & Talend Integration implementations Liaise with MuleSoft & Talend to support client implementations. Develop a product mindset and drive global template development model for global implementation. Validates solution components, leads technical guidance and provides guidance to the project manager for key issues/risks to the project Work with internal teams and business stakeholders to create prototypes, proof of concepts, etc. Lead and mentor other Integration Architects in the team. Create and own user overall Integration & Data Architecture for Integration initiatives support the Solution Architect from the Salesforce Hub(CoE). What you will bring A desire to drive your future and accelerate your career. You will bring experience and knowledge in: 10+ years CRM experience with a minimum of 5 years on the MuleSoft, Talend or any leading Integration platforms Expert & Hands On level understanding of the Integration product suite, including experience in integrating with Salesforce, SAP, GCP or AWS. Open to expand and explore Consumer Goods Domain. Experience in Consumer Goods domain will be an added advantage. Experience in being go to person for technical challenges to design and prioritise business requirements and required Capabilities. Ability to ask hard questions during sessions and suggest best practices and efficient ways of implementing business processes Proven ability to design and optimise business processes and to integrate business processes across disparate systems. Extensive experience in Integrating using MuleSoft/Talend or Other leading platforms with other Enterprise applications like Salesforce, SAP, GCP, AWS, etc with REST/SOAP APIs and Async processes. Ability to demonstrate concepts visually and in writing as the situation demands to guide stakeholders in thinking through all aspects of the ask Excellent analytical skills and the ability to develop processes and methodologies. Detail-oriented individual with the ability to rapidly learn and take advantage of new concepts, business models, and technologies. Strong background in leading large web-based systems, or complete software product lifecycle exposure Active MuleSoft certifications or ability to achieve relevant certifications upon hire Active Talend certification will be an added advantage. More about this role Work schedule: 100% No Relocation support available Business Unit Summary At Mondelēz International, our purpose is to empower people to snack right by offering the right snack, for the right moment, made the right way. That means delivering a broad range of delicious, high-quality snacks that nourish life's moments, made with sustainable ingredients and packaging that consumers can feel good about. We have a rich portfolio of strong brands globally and locally including many household names such as Oreo , belVita and LU biscuits; Cadbury Dairy Milk , Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the top position globally in biscuits, chocolate and candy and the second top position in gum. Our 80,000 makers and bakers are located in more than 80 countries and we sell our products in over 150 countries around the world. Our people are energized for growth and critical to us living our purpose and values. We are a diverse community that can make things happen-and happen fast. Mondelēz International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Job Type Regular Technology Architecture Technology & Digital
Job title: Clinical Team Manager Location: UK based, fully remote Sponsor dedicated ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Responsibilities Working fully embedded within one of our global pharmaceutical clients, with the support of ICON right behind you, you ll be at the heart of our client s innovation. As a Clinical Team Manager you will be dedicated to one of our global pharmaceutical clients who aim to use science-based innovation to deliver better patient outcomes. They aim to lead in growing areas of healthcare. The Clinical Team Manager is pivotal to trial delivery and compound development for the global R&D organization, providing leadership and driving decisions related to the conduct of a clinical trial. The CTM leads and manages the operational implementation of country feasibility, planning and delivery of R&D Phase I-IV clinical studies within and across therapeutic areas. The CTM serves as the operational point-of-contact between the Central Study Team and in-country staff aligned to the study. Accountable for high quality execution/delivery of studies within country as defined by the protocol & per agreed timelines / budget; overall project management of study activities. May provide input into the study concept, protocol, logistics and may co-ordinate other expert local input Assess appropriateness of study for local environment Conducts country/site feasibility. Leads selection of sites within country; accountable for site performance. Ensures development and maintenance of country study plan and forecast, including budgets, resource estimates, milestones, timelines, quality, and risk planning. Selects & manages local vendors in accordance with local practices & in alignment with overall resourcing strategy for the study; accountable for vendor management including oversight, agreements, payments, communications & issue management. Accountable to manage recruitment into clinical studies in accordance to relevant country commitments including contingency planning. Accountable for the creation and management of study budgets (budget updates, expenditures including site payments across a study) and reporting of accrual to finance department. With oversight; Manages the development of key study documents, plans & manuals according to local requirements (e.g., monitoring plan, local informed consent form, import/export licenses etc.); develops local recruitment and other site support materials. Ensures development of country / site-level study risk assessment to proactively identify areas at risk, develop a mitigation plan and communicate to management and study teams locally and globally. Responsible for submitting or assisting with (in accordance with local regulations and our client's standard practice) the ethics committee/IRB submissions. In some cases, may also be accountable for Regulatory Authority submissions and approvals. Arranges accurate translations of key study documentation into local language as required. Provides support / develops and negotiates Clinical Trial Agreements (depending on our client's local practices) with the investigational sites, ensuring legal input where required. Ensures necessary supplies are available at sites and manages local supply inventory. Ensures in-country study oversight: coordinates local internal & external operational activities; maintains clear visibility to sites progress and issues; reviews in-country protocol deviations; metrics; manages in-country study communications; ensures appropriate issue escalation & follow through within country and above country; communicates status/issues effectively to central team; ensures monitoring plan is followed. Build close working relationships with key partners including local medical staff. Ensures appropriate training of in-country staff and investigator sites; coordinates & delivers operational aspects at local study meetings including investigator meetings, monitor meetings and local training. Ensures the quality and integrity of clinical studies conducted in the LOC by taking on appropriate business management monitoring activities May act as a point of contact for regulatory/compliance audits of assigned study(s); provides input into LOC and site assessment/audit proposals and delivers country response & follow-up to assessment/audit reports. Accountable to specify and review in-country study monitoring tracking tools, monitors key risk and performance indicators and other reports. Review all study databases to ensure 100% accuracy. Escalates resourcing issues to ensure that in-country study activities are appropriately resourced. Ensures robust communication with sites, e.g. timely communication of protocol amendments. Reviews and approves Monitoring Visit Reports (MVRs) for their study(s) within agreed timelines to obtain an understanding of current site status. Ensures ongoing management and reporting of study specific safety issues and safety report handling, as required (including SAE reporting). Ensures conduct of assigned studies in the country according to all applicable regulations, ICH/GCP and written standards. Reviews, ensures completeness and maintains accuracy of Sponsor Study Records. Co-ordinates / contributes to end of study / program learning debriefs and identify areas for improvement. Acquires and maintains therapeutic area and product specific knowledge for the designated therapy area, study protocol training and all study related activities. Participate continuously in relevant training courses to improve personal/professional skills. Keep up to date with all the changes / required knowledge on ICH GCP, written standards and attending appropriate training sessions. Qualifications What do you need to have? Education: Undergraduate degree or its international equivalent preferably in clinical, science, or health-related field from an accredited institution; a licensed health-care professional, i.e., registered nurse Required skills 8 years of relevant experience Right to work in the UK Minimum 5 years of experience in clinical research, including a minimum of 2 years full service project management experience or an equivalent combination of education and experience sufficient to successfully perform the key responsibilities of the job. Excellent leadership skills, promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives. Demonstrates an excellent understanding of the clinical study, drug development, sample management and other associated processes and quality requirements. Strong project management mindset and demonstrated ability to work and lead in a matrix team environment involving both internal and external partners. Solid understanding of country local regulations, ICH-GCP guidelines and company written standards. Flexible and resilient with ability to evolve in changing and challenging environment. Demonstrates good English language written and verbal communication skills in addition to proven negotiation skills. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Sep 23, 2022
Full time
Job title: Clinical Team Manager Location: UK based, fully remote Sponsor dedicated ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Responsibilities Working fully embedded within one of our global pharmaceutical clients, with the support of ICON right behind you, you ll be at the heart of our client s innovation. As a Clinical Team Manager you will be dedicated to one of our global pharmaceutical clients who aim to use science-based innovation to deliver better patient outcomes. They aim to lead in growing areas of healthcare. The Clinical Team Manager is pivotal to trial delivery and compound development for the global R&D organization, providing leadership and driving decisions related to the conduct of a clinical trial. The CTM leads and manages the operational implementation of country feasibility, planning and delivery of R&D Phase I-IV clinical studies within and across therapeutic areas. The CTM serves as the operational point-of-contact between the Central Study Team and in-country staff aligned to the study. Accountable for high quality execution/delivery of studies within country as defined by the protocol & per agreed timelines / budget; overall project management of study activities. May provide input into the study concept, protocol, logistics and may co-ordinate other expert local input Assess appropriateness of study for local environment Conducts country/site feasibility. Leads selection of sites within country; accountable for site performance. Ensures development and maintenance of country study plan and forecast, including budgets, resource estimates, milestones, timelines, quality, and risk planning. Selects & manages local vendors in accordance with local practices & in alignment with overall resourcing strategy for the study; accountable for vendor management including oversight, agreements, payments, communications & issue management. Accountable to manage recruitment into clinical studies in accordance to relevant country commitments including contingency planning. Accountable for the creation and management of study budgets (budget updates, expenditures including site payments across a study) and reporting of accrual to finance department. With oversight; Manages the development of key study documents, plans & manuals according to local requirements (e.g., monitoring plan, local informed consent form, import/export licenses etc.); develops local recruitment and other site support materials. Ensures development of country / site-level study risk assessment to proactively identify areas at risk, develop a mitigation plan and communicate to management and study teams locally and globally. Responsible for submitting or assisting with (in accordance with local regulations and our client's standard practice) the ethics committee/IRB submissions. In some cases, may also be accountable for Regulatory Authority submissions and approvals. Arranges accurate translations of key study documentation into local language as required. Provides support / develops and negotiates Clinical Trial Agreements (depending on our client's local practices) with the investigational sites, ensuring legal input where required. Ensures necessary supplies are available at sites and manages local supply inventory. Ensures in-country study oversight: coordinates local internal & external operational activities; maintains clear visibility to sites progress and issues; reviews in-country protocol deviations; metrics; manages in-country study communications; ensures appropriate issue escalation & follow through within country and above country; communicates status/issues effectively to central team; ensures monitoring plan is followed. Build close working relationships with key partners including local medical staff. Ensures appropriate training of in-country staff and investigator sites; coordinates & delivers operational aspects at local study meetings including investigator meetings, monitor meetings and local training. Ensures the quality and integrity of clinical studies conducted in the LOC by taking on appropriate business management monitoring activities May act as a point of contact for regulatory/compliance audits of assigned study(s); provides input into LOC and site assessment/audit proposals and delivers country response & follow-up to assessment/audit reports. Accountable to specify and review in-country study monitoring tracking tools, monitors key risk and performance indicators and other reports. Review all study databases to ensure 100% accuracy. Escalates resourcing issues to ensure that in-country study activities are appropriately resourced. Ensures robust communication with sites, e.g. timely communication of protocol amendments. Reviews and approves Monitoring Visit Reports (MVRs) for their study(s) within agreed timelines to obtain an understanding of current site status. Ensures ongoing management and reporting of study specific safety issues and safety report handling, as required (including SAE reporting). Ensures conduct of assigned studies in the country according to all applicable regulations, ICH/GCP and written standards. Reviews, ensures completeness and maintains accuracy of Sponsor Study Records. Co-ordinates / contributes to end of study / program learning debriefs and identify areas for improvement. Acquires and maintains therapeutic area and product specific knowledge for the designated therapy area, study protocol training and all study related activities. Participate continuously in relevant training courses to improve personal/professional skills. Keep up to date with all the changes / required knowledge on ICH GCP, written standards and attending appropriate training sessions. Qualifications What do you need to have? Education: Undergraduate degree or its international equivalent preferably in clinical, science, or health-related field from an accredited institution; a licensed health-care professional, i.e., registered nurse Required skills 8 years of relevant experience Right to work in the UK Minimum 5 years of experience in clinical research, including a minimum of 2 years full service project management experience or an equivalent combination of education and experience sufficient to successfully perform the key responsibilities of the job. Excellent leadership skills, promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives. Demonstrates an excellent understanding of the clinical study, drug development, sample management and other associated processes and quality requirements. Strong project management mindset and demonstrated ability to work and lead in a matrix team environment involving both internal and external partners. Solid understanding of country local regulations, ICH-GCP guidelines and company written standards. Flexible and resilient with ability to evolve in changing and challenging environment. Demonstrates good English language written and verbal communication skills in addition to proven negotiation skills. Benefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Site Name: Rockville Vaccines, GSK House, Wavre Posted Date: Sep Job Purpose Provide global medical affairs leadership across a portfolio of pipeline assets in early stages of research and development (R&D) up to licensure, ensuring consolidated strategic medical input into R&D and commercialisation strategies. Drives the integration of insights from HCPs, patients, and the health care landscape into the asset(s) profile in alignment with the global medical accountabilities as per the GSK integrated asset operating model. Collaborative working with diverse business partners across R&D, commercial, value evidence, and regional/priority Local Operating Companies (LOCs) medical teams will be critical to ensure optimal evidence generation strategies are in place for successful registration, access, and overall launch readiness for assigned asset in early pipeline. Key Responsibilities Provides global medical affairs leadership for an assigned portfolio of assets in early development, which may include viral, bacterial, or targeted immunotherapies assets providing strategic medical insights into R&D and commercialization strategies. Responsible for strategic alignment with clinical development, central and regional partner functions, to develop and optimize the evidence generation plans in support of the scientific value proposition of assigned assets and aligns resource needs. In alignment with the Global Medical Portfolio Lead (GMPL) the GMAL will implement and lead the early GMAT and represent as appropriate the assigned assets at governance boards / meetings. Lead the creation and execution of the Global Medical Affairs Plan (MAP) and Integrated Evidence Plan (IEP) for assigned asset(s)/ indication(s). Provides medical thought leadership and therapy area expertise to strategic portfolio discussions including anticipated changes in disease landscape, treatment paradigm and evolution of Policy/Payor scenarios in key LOCs to optimize data generation and life-cycle management plans globally. Drives excellence in scientific engagement with key stakeholders (HCPs, Patients, Payers and Regulators) to gather medical insights and build a deep understanding of customer needs to inform and shape the portfolio's development programme. Provides scientific insights to validate asset and recommendation assumptions during the technical and commercial review process. Drives delivery of designated above-country elements of the MAP ensuring compliance with GSK statutory governance and documentation requirements and provide the overall framework/guidance for evidence generation activities. Develop Areas of Interest (AOIs) to support a clear (Investigator Sponsored Study) ISS program. Reviews local GSK-sponsored and ISS proposals from Key LOCs to assess their scientific merit and strategic need, liaising with R&D technical experts. Oversees strategy for medical congresses and ensure scientific points are tied to TPP. Develops and reviews publications / abstracts/ posters related to the product, key competitors and relevant disease area(s) and accountable for the Data Dissemination Plan (DDP). Responsible for ensuring plans and activities are implemented in a manner that is compliant with Scientific Engagement principles, GSK's Code of Practice and GSK values. Providing medical governance oversight for the asset, including leading the management of product-related issues/ crises with potential impact on patient safety. Ensures that all communications (internal and external) are scientifically accurate, balanced, remain aligned with product strategy, and compliant to applicable laws and regulations. Effective management of medical budget (MAP and IEP) for assigned assets. Provides direction, support and guidance to Senior medical manager and medical managers. Required qualifications and previous experience: Physician, PharmD or PhD. Significant industry and/or clinical experience in the relevant field, acquired through global/regional/Local Medical Affairs Knowledge and understanding of the development process from asset inception, early development, launch and lifecycle management. Robust understanding of GCP regulatory/ market access and reimbursement requirements. Must be able to clearly demonstrate a thorough understanding of US healthcare environment including all external stakeholders. Must be able to demonstrate understanding of medical affairs accountabilities for evidence generation, external engagement and internal advice; direct experience preferred. Must demonstrate disease area expertise and appropriate medical and/or clinical experience. Additional relevant job skills and abilities Deep knowledge of healthcare environment. Strong analytical skills to be able to assess and interpret scientific data and ability to input into the design and implementation of Phase 2 & 3b /4 studies. Highly developed leadership, networking, communication and influencing skills to work effectively in a complex matrix environment. Demonstrated ability in engaging, building and sustaining a broad and strong external (expert) network. Strong understanding and track record of adherence to the ethical, regulatory, compliance and legal framework which underpins all interactions with the external environment. Experienced communicator on scientific/medical topics in fora of different audiences, including advisory boards, public panel discussion, interaction with policy makers. Ability to be a GSK spokesperson with media. Proficient in managing multiple projects, budgets, and matrix interactions (internal / external consistent with each research project). Proven ability to strategically prioritize, deliver on time while embracing cultural diversity in complex environments. Track record of successful people management experience. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1- (US Toll Free) or +1 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf..... click apply for full job details
Sep 21, 2022
Full time
Site Name: Rockville Vaccines, GSK House, Wavre Posted Date: Sep Job Purpose Provide global medical affairs leadership across a portfolio of pipeline assets in early stages of research and development (R&D) up to licensure, ensuring consolidated strategic medical input into R&D and commercialisation strategies. Drives the integration of insights from HCPs, patients, and the health care landscape into the asset(s) profile in alignment with the global medical accountabilities as per the GSK integrated asset operating model. Collaborative working with diverse business partners across R&D, commercial, value evidence, and regional/priority Local Operating Companies (LOCs) medical teams will be critical to ensure optimal evidence generation strategies are in place for successful registration, access, and overall launch readiness for assigned asset in early pipeline. Key Responsibilities Provides global medical affairs leadership for an assigned portfolio of assets in early development, which may include viral, bacterial, or targeted immunotherapies assets providing strategic medical insights into R&D and commercialization strategies. Responsible for strategic alignment with clinical development, central and regional partner functions, to develop and optimize the evidence generation plans in support of the scientific value proposition of assigned assets and aligns resource needs. In alignment with the Global Medical Portfolio Lead (GMPL) the GMAL will implement and lead the early GMAT and represent as appropriate the assigned assets at governance boards / meetings. Lead the creation and execution of the Global Medical Affairs Plan (MAP) and Integrated Evidence Plan (IEP) for assigned asset(s)/ indication(s). Provides medical thought leadership and therapy area expertise to strategic portfolio discussions including anticipated changes in disease landscape, treatment paradigm and evolution of Policy/Payor scenarios in key LOCs to optimize data generation and life-cycle management plans globally. Drives excellence in scientific engagement with key stakeholders (HCPs, Patients, Payers and Regulators) to gather medical insights and build a deep understanding of customer needs to inform and shape the portfolio's development programme. Provides scientific insights to validate asset and recommendation assumptions during the technical and commercial review process. Drives delivery of designated above-country elements of the MAP ensuring compliance with GSK statutory governance and documentation requirements and provide the overall framework/guidance for evidence generation activities. Develop Areas of Interest (AOIs) to support a clear (Investigator Sponsored Study) ISS program. Reviews local GSK-sponsored and ISS proposals from Key LOCs to assess their scientific merit and strategic need, liaising with R&D technical experts. Oversees strategy for medical congresses and ensure scientific points are tied to TPP. Develops and reviews publications / abstracts/ posters related to the product, key competitors and relevant disease area(s) and accountable for the Data Dissemination Plan (DDP). Responsible for ensuring plans and activities are implemented in a manner that is compliant with Scientific Engagement principles, GSK's Code of Practice and GSK values. Providing medical governance oversight for the asset, including leading the management of product-related issues/ crises with potential impact on patient safety. Ensures that all communications (internal and external) are scientifically accurate, balanced, remain aligned with product strategy, and compliant to applicable laws and regulations. Effective management of medical budget (MAP and IEP) for assigned assets. Provides direction, support and guidance to Senior medical manager and medical managers. Required qualifications and previous experience: Physician, PharmD or PhD. Significant industry and/or clinical experience in the relevant field, acquired through global/regional/Local Medical Affairs Knowledge and understanding of the development process from asset inception, early development, launch and lifecycle management. Robust understanding of GCP regulatory/ market access and reimbursement requirements. Must be able to clearly demonstrate a thorough understanding of US healthcare environment including all external stakeholders. Must be able to demonstrate understanding of medical affairs accountabilities for evidence generation, external engagement and internal advice; direct experience preferred. Must demonstrate disease area expertise and appropriate medical and/or clinical experience. Additional relevant job skills and abilities Deep knowledge of healthcare environment. Strong analytical skills to be able to assess and interpret scientific data and ability to input into the design and implementation of Phase 2 & 3b /4 studies. Highly developed leadership, networking, communication and influencing skills to work effectively in a complex matrix environment. Demonstrated ability in engaging, building and sustaining a broad and strong external (expert) network. Strong understanding and track record of adherence to the ethical, regulatory, compliance and legal framework which underpins all interactions with the external environment. Experienced communicator on scientific/medical topics in fora of different audiences, including advisory boards, public panel discussion, interaction with policy makers. Ability to be a GSK spokesperson with media. Proficient in managing multiple projects, budgets, and matrix interactions (internal / external consistent with each research project). Proven ability to strategically prioritize, deliver on time while embracing cultural diversity in complex environments. Track record of successful people management experience. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1- (US Toll Free) or +1 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf..... click apply for full job details
REQ ID: 96219 JOB TITLE: Data Analytics Supervisor SALARY: Competitive LOCATION: Gaydon Hybrid Working We're re-examining our vehicles and what a vehicle means in the emerging world of automation, connectedness, electrification and the shared economy. New ideas, new technology, and new approaches to mobility are our business. Join a team of next generation thinkers. WHAT TO EXPECT As the Data Analytics Supervisor you will work within Product Engineering Operations and be responsible for the development of validation and reporting tools across JLR and provide cross-carline, cross-functional reporting and complex data analysis. You will define and translate business problems and requirements into analytics requirements and solutions. The Analytics team provide a high level of support to many areas within Engineering with data analysis and validation tool development as well as working on a wide variety of other projects, including data pipelining, process automation, metrics development and data visualisation. We work with a broad range of teams within Engineering as well as other areas of the business such as Marketing, Purchasing and Finance. The scope of work is varied and challenging. You will also be the main link between this area of the business and JLR's InDigital team and wider digital transformation strategy. This will provide technical support and training and extra resources where required by high return projects. Key Responsibilities will include: Develop and manage the delivery and optimisation of analytics solutions; ensure solution meets business needs Act as lead for development segment of larger or complex projects. During projects, takes primary accountability for day-to-day line management and capability development of developers on project team and ensures accuracy and robustness of analytics products Develop, implement and enhance analytic insights and products using a wide range of analytics tools and data engineering Design and implement data pipelines (batch/streaming) and administering running pipelines via the Google Cloud Dataflow pipeline runner Interfacing with pipeline ingress and egress mediums (Google Cloud Storage, Google Pub/Sub, Kafka via Confluent) Helping enterprise architects, software developers, and other big data engineers understand big data engineering concepts and effective usage of data pipelines by encouraging and teaching best practices Demonstrating strong problem-solving and analytical skills both individually, and as part of a group. Ability to coach and mentor other big data engineers to achieve high quality pipelines. Willingness and ability to contribute to process improvement initiatives WHAT YOU'LL NEED Essential Previous experience and knowledge of modern programming languages and scripts You will require strong experience in Python and SQL development Experience with cloud data environments such as GCP & AWS Working knowledge of data warehousing technologies such as BigQuery Familiarity with orchestration frameworks such as Apache Airflow, Luigi Excellent written and verbal communication skills Desirable: Experience of working in an Agile/XP/Scrum team and familiarity with associated techniques Knowledge of Tableau Experience programming with C or C++ is also highly desirable SO WHY US? Bring all this to the home of premium innovation, and you'll find the opportunities to further your career with a world-class team, a discounted car purchase and lease scheme for you and your family, membership of a competitive pension plan and performance related bonus scheme. All this and more makes Jaguar Land Rover the perfect place to continue your journey. This role may offer the opportunity for hybrid working where you can split your time between working from home and in the office. At Jaguar Land Rover, hybrid working is a voluntary, non-contractual arrangement providing employees with more choice and flexibility around how, when and where they work, if suitable for their role. Further details can be discussed with the Hiring Manager at interview stage. Please be aware that we may close this vacancy for applications before the stated deadline if we receive a high volume of interest. We strongly advise you to submit your application as early as possible. Jaguar Land Rover is committed to equal opportunity for all.
Sep 19, 2022
Full time
REQ ID: 96219 JOB TITLE: Data Analytics Supervisor SALARY: Competitive LOCATION: Gaydon Hybrid Working We're re-examining our vehicles and what a vehicle means in the emerging world of automation, connectedness, electrification and the shared economy. New ideas, new technology, and new approaches to mobility are our business. Join a team of next generation thinkers. WHAT TO EXPECT As the Data Analytics Supervisor you will work within Product Engineering Operations and be responsible for the development of validation and reporting tools across JLR and provide cross-carline, cross-functional reporting and complex data analysis. You will define and translate business problems and requirements into analytics requirements and solutions. The Analytics team provide a high level of support to many areas within Engineering with data analysis and validation tool development as well as working on a wide variety of other projects, including data pipelining, process automation, metrics development and data visualisation. We work with a broad range of teams within Engineering as well as other areas of the business such as Marketing, Purchasing and Finance. The scope of work is varied and challenging. You will also be the main link between this area of the business and JLR's InDigital team and wider digital transformation strategy. This will provide technical support and training and extra resources where required by high return projects. Key Responsibilities will include: Develop and manage the delivery and optimisation of analytics solutions; ensure solution meets business needs Act as lead for development segment of larger or complex projects. During projects, takes primary accountability for day-to-day line management and capability development of developers on project team and ensures accuracy and robustness of analytics products Develop, implement and enhance analytic insights and products using a wide range of analytics tools and data engineering Design and implement data pipelines (batch/streaming) and administering running pipelines via the Google Cloud Dataflow pipeline runner Interfacing with pipeline ingress and egress mediums (Google Cloud Storage, Google Pub/Sub, Kafka via Confluent) Helping enterprise architects, software developers, and other big data engineers understand big data engineering concepts and effective usage of data pipelines by encouraging and teaching best practices Demonstrating strong problem-solving and analytical skills both individually, and as part of a group. Ability to coach and mentor other big data engineers to achieve high quality pipelines. Willingness and ability to contribute to process improvement initiatives WHAT YOU'LL NEED Essential Previous experience and knowledge of modern programming languages and scripts You will require strong experience in Python and SQL development Experience with cloud data environments such as GCP & AWS Working knowledge of data warehousing technologies such as BigQuery Familiarity with orchestration frameworks such as Apache Airflow, Luigi Excellent written and verbal communication skills Desirable: Experience of working in an Agile/XP/Scrum team and familiarity with associated techniques Knowledge of Tableau Experience programming with C or C++ is also highly desirable SO WHY US? Bring all this to the home of premium innovation, and you'll find the opportunities to further your career with a world-class team, a discounted car purchase and lease scheme for you and your family, membership of a competitive pension plan and performance related bonus scheme. All this and more makes Jaguar Land Rover the perfect place to continue your journey. This role may offer the opportunity for hybrid working where you can split your time between working from home and in the office. At Jaguar Land Rover, hybrid working is a voluntary, non-contractual arrangement providing employees with more choice and flexibility around how, when and where they work, if suitable for their role. Further details can be discussed with the Hiring Manager at interview stage. Please be aware that we may close this vacancy for applications before the stated deadline if we receive a high volume of interest. We strongly advise you to submit your application as early as possible. Jaguar Land Rover is committed to equal opportunity for all.
About the role We have an exciting opportunity for a Data Engineer Manager to join an award-winning business. The Data Engineering Manager is responsible for managing the core data for the business and to help migrate it to the cloud.. Experience Proven Team Management on this field Previous experience in documenting data requirements and creating reports Proven experience in Agile (scrum) software development and technology best practice methodologies Proven experience of managing data lakes and data ingestions pipelines Knowledge of Data Governance processes Experience of big data challenges Knowledge Planning, organising & integrating: Works autonomously in planning both personal and team workload and time. Capable of prioritising workload and tasks based on business needs. Work in collaboration with all project team members, including Business analyst's, product owners, QA and DevOps Communicating & influencing skills: Excellent communication skills, both written and spoken, collaborating and working with stakeholders with the ability to explain IT issues in a way that non-technical people understand. Strong interpersonal and leadership skills: collaboration, facilitation, and negotiation skills. Ability to create good and trusted working relationships. Practical/technical knowledge: Practical experience with cloud-based systems (ideally Azure but GCP/AWS experience considered) and the relevant databases on offer (e.g. Big Query, Redshift, Azure SQL, Snowflake) Commercially focused with demonstrated ability to understand business problems and define and create robust data solutions Proven capability to implement and use different database structures Comprehensive understanding of data warehousing principles, data modelling and best practices Advanced SQL, data transformation and source data analysis skills Extensive experience of building production ETL/ELT pipelines at scale Strong problem-solving skills coupled with the ability to convey designs and ideas to a wider audience Experience of managing a small team, coaching and supporting colleagues
Sep 19, 2022
Full time
About the role We have an exciting opportunity for a Data Engineer Manager to join an award-winning business. The Data Engineering Manager is responsible for managing the core data for the business and to help migrate it to the cloud.. Experience Proven Team Management on this field Previous experience in documenting data requirements and creating reports Proven experience in Agile (scrum) software development and technology best practice methodologies Proven experience of managing data lakes and data ingestions pipelines Knowledge of Data Governance processes Experience of big data challenges Knowledge Planning, organising & integrating: Works autonomously in planning both personal and team workload and time. Capable of prioritising workload and tasks based on business needs. Work in collaboration with all project team members, including Business analyst's, product owners, QA and DevOps Communicating & influencing skills: Excellent communication skills, both written and spoken, collaborating and working with stakeholders with the ability to explain IT issues in a way that non-technical people understand. Strong interpersonal and leadership skills: collaboration, facilitation, and negotiation skills. Ability to create good and trusted working relationships. Practical/technical knowledge: Practical experience with cloud-based systems (ideally Azure but GCP/AWS experience considered) and the relevant databases on offer (e.g. Big Query, Redshift, Azure SQL, Snowflake) Commercially focused with demonstrated ability to understand business problems and define and create robust data solutions Proven capability to implement and use different database structures Comprehensive understanding of data warehousing principles, data modelling and best practices Advanced SQL, data transformation and source data analysis skills Extensive experience of building production ETL/ELT pipelines at scale Strong problem-solving skills coupled with the ability to convey designs and ideas to a wider audience Experience of managing a small team, coaching and supporting colleagues
Salary 80,000 - 90,000 GBP per year Requirements: - • 2+ years of experience working with Public Cloud Providers such as AWS, Google Cloud Platform, Azure etc. • 2+ years of experience with designing cloud implementation architectures and solutions using PaaS, DevOps & Advanced Application coding • 2+ years of experience with architecting and designing solutions using cloud technology paradigms like serverless, containers, microservices • 3+ years of experience with application transformation and modernization & data migrations projects. Demonstrated experience on multiple toolsets and adaptability to learn new tools and processes a plus. • 2+ years of experience with various Continuous Integration and Continuous Delivery (CI/CD), Source Code Repos and configuration management tools, technologies and best practices • 3+ years of experience with performing discovery and assessment of customer's overall applications portfolio, IT and business priorities and customer insights to create a modernization roadmap • 3+ years of implementation experience of cloud architectures and solutions using PaaS, DevOps & Advanced Application coding • 1+ years of experience with implementation experience of solutions using cloud technology paradigms like serverless, containers, microservices Responsibilities: - • Work closely with Dev Ops team to integrate solutions into cloud based custom developed applications • Help transform monolithic applications to a micro services framework • Support Cloud Strategy team to integrate analytical capabilities into an overall cloud architecture and business case development Technologies: - Cloud - Azure - GCP - AWS - DevOps More: Our multi-disciplinary, purpose-built team includes experts in digital and marketing strategy, service design, user interaction, technology and agile development and more. We come from industry, consultancies, digital agencies, ad agencies, creative agencies, startups, technology and development firms. Our extensive experience solving complex business, marketing, and technology problems in industries including finance, manufacturing, media and telecommunications, retail, consumer goods, transportation, government, health and life sciences, and energy brings unrivalled capability, scale, agility and acceleration to client engagements
Sep 18, 2022
Full time
Salary 80,000 - 90,000 GBP per year Requirements: - • 2+ years of experience working with Public Cloud Providers such as AWS, Google Cloud Platform, Azure etc. • 2+ years of experience with designing cloud implementation architectures and solutions using PaaS, DevOps & Advanced Application coding • 2+ years of experience with architecting and designing solutions using cloud technology paradigms like serverless, containers, microservices • 3+ years of experience with application transformation and modernization & data migrations projects. Demonstrated experience on multiple toolsets and adaptability to learn new tools and processes a plus. • 2+ years of experience with various Continuous Integration and Continuous Delivery (CI/CD), Source Code Repos and configuration management tools, technologies and best practices • 3+ years of experience with performing discovery and assessment of customer's overall applications portfolio, IT and business priorities and customer insights to create a modernization roadmap • 3+ years of implementation experience of cloud architectures and solutions using PaaS, DevOps & Advanced Application coding • 1+ years of experience with implementation experience of solutions using cloud technology paradigms like serverless, containers, microservices Responsibilities: - • Work closely with Dev Ops team to integrate solutions into cloud based custom developed applications • Help transform monolithic applications to a micro services framework • Support Cloud Strategy team to integrate analytical capabilities into an overall cloud architecture and business case development Technologies: - Cloud - Azure - GCP - AWS - DevOps More: Our multi-disciplinary, purpose-built team includes experts in digital and marketing strategy, service design, user interaction, technology and agile development and more. We come from industry, consultancies, digital agencies, ad agencies, creative agencies, startups, technology and development firms. Our extensive experience solving complex business, marketing, and technology problems in industries including finance, manufacturing, media and telecommunications, retail, consumer goods, transportation, government, health and life sciences, and energy brings unrivalled capability, scale, agility and acceleration to client engagements