Associate Director, Clinical Operations

Role: Associate Director, Clinical Operations, leading complex global early-phase oncology trials, including study setup, vendor management, and cross-functional coordination. Responsibilities: oversee study timelines, budgets, vendor relationships, and regulatory documentation; lead study teams, author/regulatory review of protocols and ICFs; monitor trial conduct ensuring GCP compliance; support regulatory strategy and site oversight; manage direct reports and contribute to SOP development. Requirements: Bachelor's in life sciences; 10+ years in clinical development with extensive oncology trial experience; strong knowledge of GCP, FDA, EMEA regulations; proven leadership in early to late-phase studies; experience managing CROs and cross-functional teams; ability to travel domestically and internationally. HighValue: oncology, early-phase, complex trial management, vendor oversight, GCP compliance, global regulatory navigation. WorkSetup: based in San Francisco, with at least 3 days/week in-office.