About this role
Regulatory Affairs Clinical Writing Professional (w/m/d) at Freseniusglobal. Location: Bad Hersfeld, Hesse, Germany. Role: Create evaluations, Ensure compliance, Collaborate cross-functional Requirements: Lead clinical evaluations, ensure EU MDR/FDA compliance, develop study protocols, collaborate cross-functionally, perform literature reviews and PMS. Category: Research and Development (R&D) Seniority: Mid Level Commitment: Full Time Workplace: Hybrid Languages: German, English