As a core member of the Medical Office team within PD, you will be instrumental in:

• Driving operational execution of clinical studies, including planning, tracking, and follow-up on key deliverables.
• Supporting site-based research and clinical partnership reviews, ensuring alignment with business priorities and regulatory standards.
• Establishing robust project structures, action trackers, and status dashboards for Clinical Partnership and Patient Safety Review Boards.
• Facilitating medical safety review processes across the product lifecycle, ensuring governance within PSQ boards.
• Collaborating cross-functionally with stakeholders in Clinical Affairs, Regulatory, Quality, Medical Safety, and Business Units.