The GCDSE provides clinical and R&D expertise, guidance and direction in the context of the region/country, in which they operate. As the leader of the Clinical (or Extended Clinical) Team, the GCDSE is the clinical representative
Primary Purpose / Regulatory Responsibilities: Collaborate with the Process Management Team members and the Product Management Team members to ensure Safety communication and product stewardship • Ensure Pharmacovigilance systems, operations and procedures are in place within
Main responsibilities Document Development Create high-quality regulatory-compliant clinical documents supporting product life cycle under supervision Ensure timely delivery while maintaining compliance with company SOPs and guidelines Innovation Learn and adopt new digital technologies, AI solutions, and efficient processes