This role leads day-to-day medical monitoring activities in support of the Chief Medical Officer (CMO), collaborates closely with the Clinical Operations team, and partners cross-functionally both internally and externally with CROs to support protocol development, study execution, and delivery of clinical milestones. Collaborate cross-functionally in the development of clinical protocols and related study documents, including but not limited to Investigator’s Brochures, development safety update reports (DSURs), informed consent forms (ICFs), protocol amendments, regulatory briefing documents, and Clinical Study Reports (CSRs).