Sr Medical Scientist - Min 3 years of previous experience in development of protocol design - English Advanced - 100% Remote

Develop medical plans including Medical Management, Data Review, and Eligibility plans by collaborating with the Medical Director and coordinating input from external experts. Perform regular and ad-hoc medical reviews of data listings and visualizations, analyzing patterns to identify risks while authoring queries and approving closures. Partner with Medical Directors for safety review meetings and slide preparation, managing project scope to ensure milestones are met. Serve as the primary interface between internal teams, customers, and vendors regarding medical data and eligibility reviews. Collaborate with Clinical Operations, Data Management, Drug Safety, and Project Management to address data integrity and subject safety concerns, escalating study issues to project leads as needed.