Overview
Senior Real World Evidence Scientist | Hybrid / Maidenhead, UK | £60 per hour
We are working with a global biopharma organisation to recruit a Senior Real World Evidence Scientist. This hands-on role is for an experienced epidemiologist who can quickly take ownership of ongoing Phase IV and post-approval studies, with a strong European focus including feasibility and evidence planning.
Key responsibilities:
1. Lead design, execution, and analysis of real-world and observational research
2. Manage ongoing Phase IV and post-approval studies and vendor/CRO activities
3. Conduct retrospective analyses using large real-world datasets (claims, EHR, registries)
4. Contribute to RWE planning and feasibility assessments across Europe
5. Support protocol development and provide technical guidance
6. Perform evidence reviews to inform regulatory, reimbursement, and strategy decisions
7. Support scientific communications, including abstracts, posters, and manuscripts
Requirements:
8. Strong background in Epidemiology/Real World Evidence within pharma or biotech
9. Experience leading both prospective Phase IV and retrospective real-world data studies
10. Proficiency with claims, EHR, or registry data and statistical tools (SAS, R, Stata)
11. Ability to work independently and take ownership of projects
12. Comfortable operating in a global, matrixed environment
Desirable:
13. Regulatory/HTA-facing RWE experience
14. Vaccines or infectious disease background
15. R programming or Shiny application experience
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