Job Title: Project Manager Internal – Clinical Evidence Planning and Evaluations
Location: Remote Duration: 1+ Years
About the Role
We are seeking a self‑driven professional to expand the impact of Medical Affairs across the organization. In this role, you will be responsible for creating and driving the clinical evidence strategy for medical devices, including Clinical Evaluation Plans and Reports (CEP/CER) and Post‑Market Clinical Evaluation Plans and Reports (PMCFP/PMCFR). You will provide clinical input to cross‑functional teams, execute Post‑Market Clinical Follow‑Up activities, and ensure compliance with EU MDR requirements.
Responsibilities
Create and drive the clinical evidence strategy for medical devices
Develop Clinical Evaluation Plans and Reports (CEP/CER) and Post‑Market Clinical Evaluation Plans ...