Regulatory & Clinical Evaluation Specialist
Role: Clinical Evaluation Specialist Consultant
Tasks:
* Writing Clinical Evaluation Plans
* Writing Clinical Evaluation Reports
* Post market Clinical Follow Up Plans & Reports
All focusing around EU Medical Device Regulation with a specific focus on Implantable Bio-materials.
Hours: Full time
Location: Hybrid in Cork, Ireland
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Writing/Editing
Industries: Medical and Diagnostic Laboratories
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