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- Tasks: Lead Risk Management activities for Clinical Trials and Medicinal Product Lifecycle.
- Company: Boehringer Ingelheim is a leading biopharmaceutical company focused on innovative therapies.
- Benefits: Enjoy excellent HR policies, health and wellbeing programs, and opportunities for personal development.
- Why this job: Join a culture that values diversity and innovation while making a real impact on lives.
- Qualifications: Master’s degree in a scientific discipline with experience in GxP and Project Management.
- Other info: Be part of a certified Top Employer committed to sustainability and global healthcare accessibility.
The predicted salary is between 43200 - 72000 £ per year.
Clinical Trials Risk Based Quality Management - 12 month Contract
You will act as an expert who leads Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle activities.
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.
- 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
- Outstanding capability and confidence to present complicated content in a clear, understandable and targeted manner
Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry’s top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need.
Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. With us, you can develop your own path in a company with a culture that knows our differences are our strengths – and break new ground in the drive to make millions of lives better.
Here, your development is our priority. Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after – as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you’ll be helping to transform lives for generations.
Clinical Trial Risk Manager employer: Boehringer Ingelheim
Contact Detail:
Boehringer Ingelheim Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Risk Manager
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in Clinical Trials Risk Management. This will not only enhance your knowledge but also demonstrate your commitment to staying updated, which is crucial for the role.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those involved in clinical trials. Attend relevant conferences or webinars to connect with potential colleagues and learn about their experiences.
✨Tip Number 3
Prepare to discuss specific examples of how you've successfully managed risks in previous roles. Highlight your analytical skills and ability to develop effective mitigation plans, as these are key aspects of the job.
✨Tip Number 4
Showcase your leadership and strategic problem-solving abilities during interviews. Be ready to explain how you can guide Business Partners and ensure compliance with stakeholder agreements in risk management.
We think you need these skills to ace Clinical Trial Risk Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials, risk management, and project management. Use specific examples that demonstrate your analytical skills and leadership capabilities.
Craft a Compelling Cover Letter: In your cover letter, express your passion for clinical trial management and how your background aligns with the role. Mention your experience with GxP and any certifications you hold that are relevant to the position.
Highlight Key Skills: Emphasise your strong computer skills and familiarity with tools like MS Office and MS Project. Provide examples of how you've used these tools to manage projects or analyse data effectively.
Showcase Problem-Solving Abilities: Include instances where you've successfully identified risks and developed mitigation plans. This will demonstrate your strategic problem-solving skills and ability to work with stakeholders.
How to prepare for a job interview at Boehringer Ingelheim
✨Showcase Your Analytical Skills
As a Clinical Trial Risk Manager, your analytical skills are crucial. Be prepared to discuss specific examples where you've successfully identified and mitigated risks in previous roles. Highlight your ability to use data from multiple sources to inform your decisions.
✨Demonstrate Leadership Experience
This role requires strong leadership capabilities. Share instances where you've led teams or projects, particularly in risk management or quality assurance. Emphasise your strategic problem-solving skills and how you've guided others in developing effective mitigation plans.
✨Familiarise Yourself with GxP Regulations
Understanding Good Practice (GxP) regulations is essential in the pharmaceutical industry. Brush up on relevant guidelines and be ready to discuss how you've applied these in your past experiences, especially in clinical trials or auditing.
✨Prepare for Technical Questions
Expect technical questions related to project management and quality risk management. Review key concepts and tools, such as MS Project and database management systems, and be ready to explain how you've used them effectively in your work.
