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 .