Senior Medical Affairs Manager

JR United Kingdom; London; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Senior Manager in Medical Affairs to drive Real-World Evidence Generation. This strategic role involves designing and executing studies that influence healthcare outcomes, collaborating with top professionals, and contributing to regulatory processes. You'll be at the forefront of innovative research, tackling real-world health challenges while expanding your leadership profile. If you're ready to make a significant impact in a global environment, this is your chance to shine and grow your career in medical affairs.

Qualifications

• Experience in real-world evidence and observational research.
• Strong communication and study management skills.

Responsibilities

• Design and execute studies on disease burden and prevalence.
• Collaborate with experts and provide scientific input for regulatory filings.

Skills

Medical Affairs

Observational Research

Communication Skills

Study Management

Statistical Tools (R, SAS, SPSS, Stata)

Education

MSc in Epidemiology

PhD in Biostatistics

MD

PharmD

Tools

R

SAS

SPSS

Stata

Job description

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Senior Manager, Medical Affairs – Real-World Evidence Generation

We're hiring on behalf of a leading multinational biopharmaceutical client for a Senior Manager in Medical Affairs, focused on Real-World Evidence (RWE) Generation. If you’re an experienced professional in medical affairs or observational research and ready to step into a strategic, cross-functional role—this is your opportunity to make an impact.

The Role

You’ll support the planning and delivery of observational research studies that help shape the future of healthcare. From study design to stakeholder engagement, you’ll bring scientific rigour and strategic insight to every project.

What You’ll Be Doing

• Design and execute studies on disease burden, prevalence, and natural history
• Support real-world evidence plans for regulators, payers, and clinicians
• Develop historical control methods and performance metrics
• Write and review study protocols, SAPs, and clinical reports
• Collaborate with internal and external experts, regulators, and advocacy groups
• Provide scientific input for regulatory filings and responses

What We’re Looking For

• MSc, PharmD, PhD or MD in a scientific field (epidemiology, biostatistics, health outcomes etc.)
• Experience in RWE, observational research, or health economics
• Strong communication and study management skills
• Knowledge of statistical tools like R, SAS, SPSS, or Stata

Bonus if you have:

• Background in oncology or haematology
• Experience in regulatory interactions and evidence generation strategy

Why Apply?

• Join a global, innovative environment tackling real-world health challenges
• Work alongside top-tier professionals across medical, clinical, and commercial teams
• Grow your leadership profile and expand your career in medical affairs and RWE

? Ready for your next step? Apply now and bring your expertise to where it matters.