Job Description
Job Summary:
- This is a senior-level RWE role within Real World Evidence (RWE) team.
- The position is opened due to a maternity leave, but the manager is open to continuing the collaboration beyond the replacement by reallocating the contractor to another mission internally.
- The role supports global RWE strategy and execution, working cross functionally with Safety, Evidence Synthesis, RWE Analysts, and multiple internal stakeholders.
- The domain is not disease specific, but dermatology experience can be an asset.
Duties and Responsibilities:
- Lead and execute complex RWE studies (epidemiology, natural history, PASS/PAES, regulatory studies, external control arms, comparative effectiveness).
- Develop study concepts, protocols, SAPs, and ensure governance compliance.
- Interpret study results and communicate insights internally and externally.
- Collaborate with RWE Analysts, BQS, Safety, Evidence Synthesis, external vendors, and cross functional teams.
- Identify innovative designs, new data sources, and advanced analytics opportunities.
- Contribute to the RWE functional strategic plan with the RWE Strategy Lead.
Education and Experience:
- Master’s or PhD in Epidemiology (PhD preferred).
- Strong experience with real world data and RWE project execution.
- Strong quantitative/methodological background (epidemiology, biostatistics, pharmacoepidemiology, outcomes research).
- Experience communicating RWE results to diverse internal/external stakeholders.
- Ability to work cross functionally and autonomously in a senior role.
- Pharma experience (strong preference) — critical for understanding business needs and interacting effectively with internal functions (manager insight).
Years of Experience:
- Several years of proven experience in designing and delivering RWE projects (industry, consultancy, or academic center of excellence).
- Seniority required: ability to lead high complexity studies and engage effectively with cross functional stakeholders.
- Manager strongly prefers candidates with prior pharmaceutical industry experience.
- Skilled in scientific dissemination (abstracts, posters, manuscripts).
- Demonstrated ability to innovate and propose advanced methodological approaches.
- Able to challenge and defend methodological choices confidently with stakeholders.
Nice to Have:
- Experience in Dermatology (not required but preferred when comparing similar profiles).
- Experience with hybrid study designs, external control arms, or regulatory driven RWE projects.
Language Requirements:
- Excellent English (written and spoken) required.