Job Description
Job Description If you're someone who genuinely enjoys owning clinical trials from start to finish and takes pride in keeping complex studies running smoothly, this could be a great fit. We're looking for a Clinical Research Program Manager who brings strong experience in clinical trial operations-someone who understands what it takes to move a study forward from start-up through closeout. You'll be stepping into a collaborative, supportive team environment where your expertise in multi-site trial management, protocol and database development, and overall study lifecycle execution will be valued and relied on. To set you up for success, we're looking for at least five years of clinical trial management experience, including three years leading multi-site studies. In this role, you'll partner closely with CROs, vendors, and cross-functional teams, building strong relationships that help drive studies forward with clarity and efficiency. This is a growing department, so there's real opportunity to shape how work gets done, contribute ideas, and expand your impact over time. If you're looking for a place where your experience is respected, your voice matters, and your career can continue to grow alongside a strong team, we'd be glad to connect. Responsible for directing and managing Cedars-Sinai's multi-site clinical coordinating center. Provides leadership, guidance and direction for the day-to-day clinical research operations and activities, including authority to make independent decisions regarding program operations, administration, and governance. Ensures compliant, efficient, and effective conduct of the clinical trials within the portfolio. Establishes, implements, and evolves operational standards and monitors quality and progress of the clinical coordinating center. Primary Duties and Responsibilities Oversees and/or manages a multi-site clinical coordinating center with