
The Clinical Development Scientist Manager role supports scientific oversight and data integrity for Internal Medicine clinical trials within a global pharmaceutical team. Key responsibilities include contributing to protocol development and amendments, reviewing safety data and adverse events, managing clinical data quality, and supporting regulatory submissions and audits. The position offers the opportunity to work on pivotal Phase 3 studies in cardiometabolic diseases while collaborating with cross-functional teams and external stakeholders. This hybrid role provides a dynamic environment focused on continuous process improvement and innovative trial execution, with potential for global travel to support study sites and investigator meetings.




















