Clinical Trials Risk Manager

Clinical Trials Risk Based Quality Management – 12 month Contract

Role Overview

You will act as an expert leading Risk Management activities for Clinical Trials and other Medicinal Product Lifecycle activities.

Tasks & Responsibilities

1. Lead Risk Assessment, Review, Control, and Reporting activities with Key Stakeholders in Clinical Trial Teams and partners.
2. Utilize data from multiple sources to identify Quality Risks.
3. Assist Business Partners in developing mitigation plans and oversee their implementation.
4. Report Clinical Trial risk management information to Key Stakeholders throughout the Product Lifecycle.

Requirements

• Master’s degree in a scientific discipline with experience in GxP within the pharmaceutical industry.
• Experience with clinical trials, clinical research, clinical trial management, or auditing is a plus.
• Knowledge in Project Management and Quality Risk Management.
• Leadership and strategic problem-solving skills, with good process and quality management knowledge.
• Strong computer skills, including MS Office, MS Project, and database tools.
• Excellent organizational skills and multitasking ability.
• Ability to communicate complex information clearly and effectively.

Why Join Boehringer Ingelheim

Boehringer Ingelheim is recognized as a Top Employer in the UK, committed to a better world of work through excellent HR policies and practices.

We focus on developing innovative therapies in human and animal health, investing heavily in R&D, and embedding sustainability across our value chain. With approximately 54,500 employees serving over 130 markets, we aim to build a healthier and more sustainable tomorrow.

Join us to develop your career in a culture that values diversity, innovation, and employee wellbeing. We offer a respectful, friendly environment where everyone is valued and supported in their professional growth.

Learn more about us at our website.

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