Associate Director, Clinical Study Management, EMEA/LATAM

Role: Associate Director, Clinical Study Management, EMEA/LATAM, overseeing global clinical trials primarily in oncology, ensuring operational excellence and compliance. Responsibilities: lead multi-center Phase I–IV studies, manage timelines, budgets, cross-functional teams, and vendors; ensure adherence to ICH-GCP, regional regulations, and company standards; oversee study documentation, resource planning, and stakeholder updates; support team growth and regional operational improvements. Requirements: 10+ years of clinical trial management experience, Bachelor’s or higher degree; fluency in English, additional EMEA/LATAM languages a plus; deep knowledge of ICH-GCP, regional guidelines, and regulatory landscapes; proven track record in managing complex global trials within timelines and budgets; strong leadership, communication, and organizational skills; experience with budget, resource, and KPI management. HighValue: regional trial oversight in oncology, international experience in Phases I–IV, regulatory compliance expertise, vendor and stakeholder management, team leadership, and study document control. WorkSetup: onsite minimum 3 days/week in Jersey City or Millbrae; travel requirements not specified but likely related to trial sites.