Job description
The Associate Director, Global Trial Lead will lead global clinical trials with expertise in planning, execution, and oversight. They will ensure regulatory compliance, patient safety, and timely delivery of high-quality data. The role involves a combination of execution and oversight, dependent on the sourcing model, to ensure deliverables.
Responsibilities include project management, study input and strategic guidance, budgeting and resource planning, and program and study oversight. The Associate Director will lead cross-functional teams, manage end-to-end trial operations, and oversee budgets and forecasts.
The ideal candidate will have a BA/BS or equivalent degree in a relevant discipline, with a minimum of 7 years of experience in clinical operations roles and project management in the pharmaceutical or healthcare industry. They will have experience in independently leading complex global clinical trials and leading global and multi-functional teams.
Company
Healthcare
Bristol‑Myers Squibb (BMS) is a global biopharmaceutical leader dedicated to discovering, developing, and delivering innovative medicines that address serious diseases such as cancer, immunologic disorders, cardiovascular conditions, and fibrosis. Leveraging deep scientific expertise and a robust pipeline of novel therapies, BMS combines cutting‑edge research with rigorous clinical development to bring transformative treatments to patients worldwide. The company’s value proposition lies in its commitment to scientific excellence, patient‑focused outcomes, and collaborative culture, offering employees the opportunity to contribute to breakthrough medicines that improve lives. BMS provides a dynamic environment for professionals seeking to advance their careers in drug discovery, clinical research, regulatory affairs, and commercial operations while making a meaningful impact on global health.
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B.M.S.
Bristol Myers Squibb
Bristol Myers Squibb
Bristol Myers Squibb
Bristol Myers Squibb
Bristol Myers Squibb