Collaborate cross-functionally in the development of clinical protocols and related study documents, including but not limited to investigator brochures (IBs), development safety update reports (DSURs), informed consent forms (ICFs), protocols, protocol amendments, and Clinical Study Reports (CSRs). This role leads medical monitoring activities, collaborates closely with the CMO and clinical ops team, and partners cross-functionally both internally and externally with CROs to support protocol development, study execution, and delivery of clinical milestones.