Associate Director, Clinical Operations

Role: Associate Director of Clinical Operations leading early-stage oncology clinical trials. Responsibilities include developing clinical strategies, managing site and CRO relationships, overseeing study timelines, and ensuring GCP compliance. The candidate will serve as the program lead, collaborating cross-functionally on protocol development, safety reports, regulatory submissions, and data management. Requirements: minimum 8 years of clinical operations experience across at least two therapeutic areas, including oncology; experience managing CROs and vendors internationally; familiarity with drug development stages from IND to NDA; strong communication and leadership skills; experience with biomarker-driven studies preferred. HighValue: oncology, early-stage clinical trials, CRO/vendor management, international trials, GCP compliance, cross-functional collaboration. WorkSetup: not specified.