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:
- Lead design, execution, and analysis of real-world and observational research
- Manage ongoing Phase IV and post-approval studies and vendor/CRO activities
- Conduct retrospective analyses using large real-world datasets (claims, EHR, registries)
- Contribute to RWE planning and feasibility assessments across Europe
- Support protocol development and provide technical guidance
- Perform evidence reviews to inform regulatory, reimbursement, and strategy decisions
- Support scientific communications, including abstracts, posters, and manuscripts
Requirements:
- Strong background in Epidemiology/Real World Evidence within pharma or biotech
- Experience leading both prospective Phase IV and retrospective real-world data studies
- Proficiency with claims, EHR, or registry data and statistical tools (SAS, R, Stata)
- Ability to work independently and take ownership of projects
- Comfortable operating in a global, matrixed environment
Desirable:
- Regulatory/HTA-facing RWE experience
- Vaccines or infectious disease background
- R programming or Shiny application experience
Please apply direct or send your CV to julie.ball@cpl.com.