Associate Director, Clinical Study Management, EMEA/LATAM

Role: Associate Director, Clinical Study Management (EMEA/LATAM), overseeing global clinical trials primarily in oncology, with a focus on operational excellence, regulatory compliance, and team leadership. Responsibilities: lead multi-center Phase I–IV trials, manage regional vendors and internal resources, ensure adherence to ICH-GCP, EMEA, and LATAM regulations, coordinate study documentation, and oversee regional budgets and KPIs; hire and develop regional clinical operations staff; provide regular stakeholder updates and contribute to process improvements. Requirements: 10+ years of clinical trial management experience (or 8+ years with postgraduate degree), deep knowledge of GCP, regional regulations, and experience managing global trials; strong leadership, communication, and organizational skills; fluency in English, with additional EMEA/LATAM languages a plus. HighValue: global multi-center trials, oncology, Phase I–IV, regional regulatory expertise, vendor management, team leadership in clinical operations, working onsite 3+ days/week in Jersey City or Millbrae. WorkSetup: hybrid onsite; travel as needed.