Opportunity Description
Role Overview
This position will execute and communicate high‑quality observational studies. The role is cross‑functional, partnering with clinical, regulatory, biometrics, safety, and commercial teams to deliver impactful evidence that supports decision‑making across the organisation.
Key Responsibilities:
- Execution of observational research across early and late‑stage development.
- RWE support for regulators and payers including registries and burden‑of‑illness work.
- Development of RWE methodologies including historical controls and analytical approaches.
- Performance tracking through dashboards and project metrics.
- Cross‑functional communication of complex observational methods to diverse audiences.
- Stakeholder management across internal teams and external experts.
- Protocol and document writing including protocols, SAPs, and clinical study reports.
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