Project Manager Internal
The Judge Group
Operations
Remote
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 and Reports (PMCFP/PMCFR)
Provide clinical input to cross‑functional teams on development, risk management, product management, and surveillance
Execute Post‑Market Clinical Follow‑Up activities (surveys, literature searches, clinical studies)
Review promotional materials and claims for accuracy and compliance
Qualifications
Master’s or PhD in Medical Physics (preferred), Biophysics, Biomedical Engineering, or related field
2–5 years of experience in clinical evaluations, medical physics, or related field
Strong understanding of Clinical Evaluation and Post‑Market Clinical Follow‑Up requirements for Class I–III medical devices under EU MDR
Familiarity with medical device design and manufacturing, especially in radiation oncology
Excellent technical writing and verbal communication skills
Ability to work autonomously in a remote environment