Serve as medical monitor for clinical trials.
Partner with study team on design, feasibility, and site selection.
Review protocols, safety plans, charters, and ICFs.
Collaborate with Regulatory Affairs on investigator brochures and briefs.
Lead investigator meetings and site initiation visits.
Work cross-functionally with discovery, operations, regulatory, safety, and CROs.
Oversee safety and efficacy data gathering, analysis, and reporting.
Support publications and external communications; present at meetings.

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