Clinical Team Manager (CTM) – HemOnc

Clinical Trial Manager responsible for leading clinical operations and quality management for low-to-moderate complexity studies in HemOnc. Drives delivery of final clinical deliverables per contract, ensures compliance with ICH GCP, develops and implements tools (e.g., Monitoring Plan, CRF guidelines), prepares trial documentation (TMF content, ethics submissions), and collaborates across departments to maintain timelines, budgets, and quality. Schedules and leads team meetings, oversees data quality plans, monitors CRF collection and query resolution, and may participate in start-up activities and regulatory submissions. Requires a Bachelor’s degree (or equivalent) and 5+ years of related experience; strong leadership, planning, budgeting, and cross-functional collaboration skills; proficient in English; familiar with FDA guidelines and regulatory expectations. Frequent domestic and international travel is expected.