Clinical Trial Manager III

The Clinical Trial Manager III leads the full lifecycle management of clinical research studies, ensuring timely and compliant execution from site identification through database lock. This role owns end-to‑end oversight of start‑up activities, including site selection, activation, and the development and translation of informed consent forms, as well as the creation and collection of essential documents such as insurance and site budgets. The manager negotiates and executes Clinical Trial Agreements, coordinates regulatory and ethics committee submissions, and oversees the logistics of ancillary supplies, import/export processes, and supply destruction. Financial responsibilities include revenue forecasting, adherence to contracted scope, and managing scope modifications while tracking key project indicators specific to each client. The position also involves proactive risk management, budget oversight, and ensuring that project team resources are accurately projected and allocated. Additionally, the manager develops and implements site activation and recruitment strategies, leads monitoring visit planning, and maintains compliance with SOPs, client requirements, and regulatory standards throughout the study.

Source: Himalayas