Real World Evidence
3 days ago
Maidenhead
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.