Description
The ESR Manager serves as the operational backbone for externally sponsored research in the United States, coordinating external and internal stakeholders, governance, contracts, budgets, systems, compliance, risk mitigation, and study performance. The role manages ESR processes across assigned tumor types, supports regulatory submissions, maintains study and portfolio data, and ensures studies are delivered on time, on budget, and inspection-ready. Candidates need a bachelor’s degree in a scientific or healthcare field or comparable experience, 1–2+ years of pharmaceutical industry experience, study-management-system experience, and knowledge of clinical study and drug-development processes.
