Develops, writes, and manages high-quality clinical and regulatory documents for global standards, collaborating cross-functionally to maintain clinical documentation within the Quality Management System.
Requirements
- Author and edit clinical documents
- Plan and report clinical data collection
- Ensure clinical documentation compliance
- Collaborate with Global Regulatory & Clinical Affairs teams
- Stay updated on scientific literature and regulatory changes
- Participate in cross-functional projects
- Support Medical Affairs for literature reviews and writing of documentation
