Job Description

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, R...

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