Medical Affairs Specialist

3 days ago


Stockholm, Stockholm, Sweden PharmaRelations ApS Full time
Key Responsibilities
  1. Study Coordination: Ensure studies are on track for site initiation, patient recruitment and enrollment, and take corrective actions where necessary to address issues.
  2. Agreement Management: Conduct the coordination and follow-up of CC agreements (Investigator Initiated Study agreements, etc.) with technical and clinical collaboration contacts.
  3. Post-Market Research: Manage and execute post-market clinical research studies and surveys.
  4. Regulatory Compliance: Ensure compliance with legal and regulatory requirements (e.g., GCP, ISO standards, MDR, and CFR/FDA).


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