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Consultant – RWE Project Manager, Medical Devices
Ividata Life SciencesConsultant Chef de projet RWE / Dispositifs Médicaux chez IVIDATA Life Sciences. Intégration dans un environnement d'innovation en santé avec des experts passionnés à Paris.
About the role
Key responsibilities & impact- Lead and coordinate PMCF (Post-Market Clinical Follow-up) data collection
- Design and implement simple post-market clinical studies
- Draft study protocols, case report forms (CRFs), and final clinical study reports
- Ensure collected data comply with the MDR (EU Medical Device Regulation 2017/745) requirements
- Provide methodological support to investigator physicians
- Manage timelines, monitor enrollments, and liaise with hospitals and clinical sites
- Lead regulatory activities and necessary submissions
Requirements
What you’ll need- Minimum 4 years of clinical project management experience, ideally in the medical devices sector
- Strong understanding of PMCF requirements under the EU Medical Device Regulation (MDR)
- Ability to collaborate with domain experts and provide methodological support
- Fluent English (for international contexts and scientific writing)
Benefits
Comp & perks- Stimulating work environment
- High-impact assignments
- Remote work possible
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical project managementdata collectionstudy protocol draftingcase report forms (CRFs)clinical study reportsregulatory submissionspost-market clinical studiesmethodological support
Soft Skills
collaborationcommunicationleadershiporganizational skills