Associate Director, Clinical Operations

The Associate Director, Clinical Operations serves as leadership role within the Clinical Operations department under the supervision of Senior Director, Clinical Operations, is responsible for the execution planning and conduct of clinical trials. This requires deep operational expertise to ensure trials are conducted in compliance with regulatory and ethical requirements, timelines, and budgetary constraints, and of the quality required to support submission to relevant authorities for drug approval. Key Responsibilities include: Conduct end-to-end clinical trial management, lead early feasibility efforts, develop clinical trial/program budgets, develop timelines for assigned clinical trials, develop Request for Proposals (RFPs), identify and escalate project risks, monitor performance of CROs, partner with other functions to optimize study design, contribute to clinical content of essential documents, interact with clinical trial investigators and key opinion leaders.