About the Role
A leading global biotechnology organisation is building a new Safety Evidence Generation function and is seeking an experienced Epidemiologist / Pharmacoepidemiologist Consultant to support real-world safety studies across its innovative therapy portfolio.
This is a high-impact contract role focused on generating post-authorisation safety evidence using real-world data sources.
Key Responsibilities- Design and execute pharmacoepidemiology studies addressing key safety research questions
- Lead post-authorisation safety studies (PASS/PAS) and real-world safety evidence generation
- Identify appropriate methodologies and data sources (claims, EHR, registries, external databases)
- Develop study concepts, protocols, statistical analysis plans, and study reports
- Interpret safety findings, identify evidence gaps, and support strategic safety insights
- Collaborate cross-functionally with Medical Affairs, Regula...
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