Clinical Project Manager

Job Summary

To expand the impact of Medical Affairs, the contract Project Manager Internal will create and drive the clinical evidence strategy for medical devices, including Clinical Evaluation Plans and Reports, while working remotely for a duration of over one year.

Key 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)
• Execute Post Market Clinical Follow Up activities, including surveys and literature searches

Required qualifications

• Master's or PhD in Medical Physics, Biophysics, Biomedical Engineering, or related field
• 2-5 years of experience in clinical evaluations 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, particularly in radiation oncology
• Ability to work autonomously in a remote environment