Manager, Clinical Risk and Analytics

Alnylam Pharmaceuticals; United Kingdom; Remote; GBP 50,000 - 75,000; Full time

Job summary

A leading pharmaceutical company is seeking a Manager in Clinical Risk and Analytics to drive innovation in clinical trials. This role involves implementing Risk-Based Quality Management strategies, managing study risks, and ensuring safety and quality in trials. Candidates should possess extensive experience in clinical research and strong analytical skills, ready to thrive in a dynamic team environment.

Qualifications

• Proven end to end clinical trials experience required.
• Strong understanding of clinical development processes.
• Expertise in clinical trial risk management and centralized monitoring.

Responsibilities

• Conduct and manage Study Risk Assessments periodically.
• Develop centralized monitoring plans and review setups.
• Guide teams on systemic risks and follow up on actions.

Skills

Analytical skills

Critical thinking

Project management

Education

Degree in a scientific, analytical, or technical discipline

Job description

2128: Manager, Clinical Risk and Analytics

Location: Virtual, UK

Are you passionate about driving innovation in clinical trials through smart, data-driven risk management? At Alnylam, we're changing the future of medicine through our revolutionary RNAi technology - and we're looking for exceptional talent to join us on this journey.

We're offering an exciting opportunity for an outstanding Clinical Risk and Analytics professional to join our dynamic Clinical Risk and Analytics team. As part of the wider Data Science, Statistics & Epidemiology group, this team plays a vital role in ensuring the safety, integrity, and quality of our clinical trials through expert risk management (RM) and centralized monitoring (CM).

What You'll Do......

In this pivotal role, you'll be at the forefront of implementing Risk-Based Quality Management (RBQM) strategies across our studies - from study design through to closeout. Each RBQM Lead is empowered to manage their program across all trial phases, supported by a highly skilled team of analysts and programmers. If you're ready to make a real impact in a collaborative, forward-thinking environment where data meets purpose, we'd love to hear from you.

Key Responsibilities
• Conduct and manage Study Risk Assessment at start and periodically
• Develop the centralized monitoring plan
• Review centralized monitoring study set up for study team.
• Review findings from CM and review with study team for action
• Follow up on actions, and guide teams on systemic risks

About you...

You'll bring a strong foundation in clinical research in the pharmaceutical or CRO industry. With a degree (or equivalent) in a scientific, analytical, or technical discipline, you have a solid understanding of clinical development processes and are confident in the concepts of study design, conduct, and closeout. Your expertise in clinical trial risk management-paired with your familiarity with centralized monitoring and RBQM principles-positions you to contribute meaningfully from day one.

Equally important is your ability to work collaboratively within a dynamic team, managing shifting priorities while maintaining focus on shared goals. You communicate clearly and effectively in English, both in writing and verbally, and are comfortable navigating complex information to deliver high-quality insights and outcomes. If you're a proactive problem-solver who thrives in a fast-paced, science-driven environment, you could be the ideal fit for our team.

You will have...

Essential Skills & Experience
• Proven end to end clinical trials experience
• Strong critical thinking and analytical skills, and Aptitude for data analytics
• Good understanding and knowledge of risk management concepts and principles
• Excellent project management capabilities

Desirable Skills & Experience
• Experience and good understanding of clinical trial data from various sources (e.g. Clinical devices, SDTM, RAVE, IRT, etc.)
• Knowledge of Good Clinical Practice/ICH E6 (R3), ICH E8 R1 Guidelines and/or other applicable regulatory requirements
• High degree of accuracy and attention to detail

Are you ready to be part of what's next? Join us and help bring groundbreaking RNAi therapies to patients around the world.

Next Steps

This vacancy will be advertised from Monday, 26th May with a scheduled closing date of Friday, 30th May - we welcome your application as soon as possible.

Additional Resources

Working at Alnylam: https://www.alnylam.com/careers/working-at-alnylam

Who We Are: https://www.alnylam.com/careers/who-we-are