Job Description: The Data Analytics Operations Manager will lead Risk Management activities for Clinical Trials and Medicinal Product Lifecycle activities, focusing on Risk Based Quality Management. This role involves guiding Business Partners in risk assessment, mitigation planning, and reporting to Key Stakeholders. The position requires strong analytical skills and the ability to manage multiple tasks effectively. A Master's degree in a scientific discipline and experience in the pharmaceutical industry are essential for success in this role.
Key Responsibilities:
- Lead Risk Assessment, Review, Control, and Reporting activities for Clinical Trials.
- Utilize data from multiple sources to identify Quality Risks.
- Guide Business Partners in developing and implementing mitigation plans.
- Report Clinical Trial risk management information to Key Stakeholders.
Skills Required:
- Master’s degree in a scientific discipline.
- Experience in GxP within the pharmaceutical industry.
- Proficient in clinical trials and clinical research management.
- Knowledge in Project Management and Quality Risk Management.
- Strong leadership and strategic problem-solving skills.
- Excellent organizational skills and ability to manage multiple tasks.
- Strong computer skills, including MS Office and MS Project.
- Ability to present complex information clearly.
Salary (Rate): undetermined
City: Bracknell
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Data Analytics Operations Manager - Product Development Quality Risk Management 12 month Contact
As a Data Analytics Operations Manager you will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle activities.
Tasks & responsibilities
Imagine yourself at the heart of Risk Based Quality Management for Clinical Trials in support of Medicinal Product Development and throughout the Product Lifecycle. Picture yourself leading Risk Assessment, Review, Control and Reporting activities with Key Stakeholders in Clinical Trial Teams and other partners within the organization. Visualize utilizing up-to-date data from multiple sources to identify Quality Risks. Your analytical skills will be crucial in assisting Business Partners in this task. Envision yourself guiding Business Partners in developing mitigation plans to address identified risks and ensuring implementation and oversight according to Stakeholder agreements. Consider being responsible for reporting Clinical Trial risk management information to Key Stakeholders throughout the Product Lifecycle.
Requirements
- Master’s degree in scientific discipline with a few years of experience in GxP within pharmaceutical industry
- Proficient experience with clinical trials, clinical research associate, clinical trial management, or clinical auditing considered a plus
- Proven knowledge in Project Management including experience in Quality Risk Management
- Demonstrated experience in leadership and strategic problem-solving paired with good knowledge about processes and quality management
- Strong computer skills, including MS Office, MS Project, database tools, and the talent to quickly learn new systems
- Excellent organizational skills and ability to accomplish multiple tasks of varied complexity simultaneously
- Outstanding capability and confidence to present complicated content in a clear, understandable and targeted manner
WHY THIS IS A GREAT PLACE TO WORK
Boehringer Ingelheim has been recognised as a Top Employer in the UK. Being certified as a Top Employer confirms our dedication to a better world of work, delivered through excellent HR policies and people practices.
To learn more visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
Our Company
At Boehringer Ingelheim we develop breakthrough therapies that improve the lives of both humans and animals. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective. Now, we are powered by 52,000 employees globally who nurture a diverse, collaborative and inclusive culture. We believe that if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve.
Why Boehringer Ingelheim?
With us, you can grow, collaborate, innovate and improve lives. We offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. In addition, learning and development for all employees is key, because your growth is our growth. Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients and communities.
Want to learn more? visit https://www.boehringer-ingelheim.com
Negotiable
Bracknell, England, United Kingdom
Undetermined
Undetermined
Other
Not Specified
Job Description: The Data Analytics Operations Manager will lead Risk Management activities for Clinical Trials and Medicinal Product Lifecycle activities, focusing on Risk Based Quality Management. This role involves guiding Business Partners in risk assessment, mitigation planning, and reporting to Key Stakeholders. The position requires strong analytical skills and the ability to manage multiple tasks effectively. A Master's degree in a scientific discipline and experience in the pharmaceutical industry are essential for success in this role.
Key Responsibilities:
- Lead Risk Assessment, Review, Control, and Reporting activities for Clinical Trials.
- Utilize data from multiple sources to identify Quality Risks.
- Guide Business Partners in developing and implementing mitigation plans.
- Report Clinical Trial risk management information to Key Stakeholders.
Skills Required:
- Master’s degree in a scientific discipline.
- Experience in GxP within the pharmaceutical industry.
- Proficient in clinical trials and clinical research management.
- Knowledge in Project Management and Quality Risk Management.
- Strong leadership and strategic problem-solving skills.
- Excellent organizational skills and ability to manage multiple tasks.
- Strong computer skills, including MS Office and MS Project.
- Ability to present complex information clearly.
Salary (Rate): undetermined
City: Bracknell
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Data Analytics Operations Manager - Product Development Quality Risk Management 12 month Contact
As a Data Analytics Operations Manager you will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle activities.
Tasks & responsibilities
Imagine yourself at the heart of Risk Based Quality Management for Clinical Trials in support of Medicinal Product Development and throughout the Product Lifecycle. Picture yourself leading Risk Assessment, Review, Control and Reporting activities with Key Stakeholders in Clinical Trial Teams and other partners within the organization. Visualize utilizing up-to-date data from multiple sources to identify Quality Risks. Your analytical skills will be crucial in assisting Business Partners in this task. Envision yourself guiding Business Partners in developing mitigation plans to address identified risks and ensuring implementation and oversight according to Stakeholder agreements. Consider being responsible for reporting Clinical Trial risk management information to Key Stakeholders throughout the Product Lifecycle.
Requirements
- Master’s degree in scientific discipline with a few years of experience in GxP within pharmaceutical industry
- Proficient experience with clinical trials, clinical research associate, clinical trial management, or clinical auditing considered a plus
- Proven knowledge in Project Management including experience in Quality Risk Management
- Demonstrated experience in leadership and strategic problem-solving paired with good knowledge about processes and quality management
- Strong computer skills, including MS Office, MS Project, database tools, and the talent to quickly learn new systems
- Excellent organizational skills and ability to accomplish multiple tasks of varied complexity simultaneously
- Outstanding capability and confidence to present complicated content in a clear, understandable and targeted manner
WHY THIS IS A GREAT PLACE TO WORK
Boehringer Ingelheim has been recognised as a Top Employer in the UK. Being certified as a Top Employer confirms our dedication to a better world of work, delivered through excellent HR policies and people practices.
To learn more visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
Our Company
At Boehringer Ingelheim we develop breakthrough therapies that improve the lives of both humans and animals. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective. Now, we are powered by 52,000 employees globally who nurture a diverse, collaborative and inclusive culture. We believe that if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve.
Why Boehringer Ingelheim?
With us, you can grow, collaborate, innovate and improve lives. We offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. In addition, learning and development for all employees is key, because your growth is our growth. Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients and communities.
Want to learn more? visit https://www.boehringer-ingelheim.com

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