Real World Evidence

Job description

Real World Evidence Scientist (Contract)

CPL Life Sciences are recruiting for RWE Scientist for a leading pharmaceutical company based in Berkshire. This role is required to provide temporary coverage for a team member on an initial 12 month contract.

• 12 month contract
• Hybrid in Berkshire
• Programming experience required

This individual role requires a hands-on epidemiologist who can independently lead ongoing Phase IV and post-approval real-world evidence studies. The position includes EU-focused feasibility and evidence planning activities and operates within a global team, collaborating closely with the data and medical affairs departments.

Key Responsibilities:

• Lead design, execution, and analysis of Phase IV and observational RWE studies
• Assume ownership of post-approval epidemiologic studies
• Oversee CROs and vendors to ensure quality, timelines, and regulatory compliance
• Conduct retrospective analyses using large claims, EHR, and registry data sources
• Develop protocols and statistical analysis plans with methodological rigor
• Lead EU-focused feasibility assessments and contribute to RWE strategy
• Perform evidence reviews, systematic literature reviews, and meta-analyses
• Support regulatory-/HTA-facing deliverables and post-approval commitments
• Contribute to scientific communication (abstracts, posters, manuscripts)

The ideal candidate brings epidemiology/RWE experience, strong statistical programming skills (SAS/R), and the ability to work independently with minimal ramp-up in a fast-paced, global setting.

Extra information

Status

Open

Education Level

Secondary School

Location

Maidenhead

Type of Contract

Full-time jobs

Published at

04-03-2026

Full UK/EU driving license preferred

No

Car Preferred

No

Must be eligible to work in the EU

No

Cover Letter Required

No

Languages

English