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Job Description
- Manage the end-to-end execution of clinical trial activities, including protocol development, Institutional Review Board submissions, site initiation/training, and study monitoring which may include some travel (5-10%).
- Coordinate technical readiness for clinical studies, including custom research app deployment, user setup, clinical data management, and protocol compliance.
- Build cross-functional consensus and independently manage dependencies, risks, and mitigation plans across software engineering, product, regulatory, legal, and privacy teams.
- Design and track program operations, utilizing internal dashboards, metrics, and AI/ML productivity tools to drive continuous process improvements.
- Establish scalable operational processes for managing clinical vendors, agreements, and purchase orders.