Clinical Documentation Expert

2 days ago


Stockholm, Stockholm, Sweden ProPharma Full time
Job Summary
ProPharma is looking for a Clinical Documentation Expert to join our team. As a key contributor to our regulatory writing team, you will be responsible for creating high-quality clinical documentation that meets client and regulatory agency requirements. You will work closely with cross-functional teams to ensure that all documentation is accurate, complete, and compliant with relevant regulations.

Responsibilities
  • Create high-quality clinical documentation, including clinical, safety, regulatory, device, diagnostics, or disclosures documents.
  • Collaborate with subject matter experts in clinical operations, data management, biostatistics, regulatory affairs, etc., as needed.
  • Maintain familiarity with current industry practices, regulatory requirements, and guidelines related to regulatory writing.


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