Senior Clinical Trial Manager

Role: Senior Clinical Trial Manager overseeing global oncology Phase 2/3 trials, including NSCLC and colorectal cancer, with responsibilities spanning study start-up to closeout, CRO oversight, and inspection readiness. The role involves strategic leadership in site selection, enrollment, monitoring, risk management, and data quality, ensuring regulatory compliance and quality standards (GCP, ICH). Responsibilities include developing study plans, managing CRO activities, leading risk mitigation, and mentoring clinical operations staff. Requirements: Bachelor's in life sciences or related field; 8–10+ years in clinical operations, with at least 7+ years managing international oncology trials at Phase II/III; proficiency in clinical data review, regulatory interactions, and vendor oversight; ability to travel up to 20%. Preferred skills include deep knowledge of drug development, GCP, and ICH guidelines, leadership in complex studies, and excellent organizational and communication skills. High-value specifics: Oncology (NSCLC, CRC), Phase 2/3, international scope, CRO management, inspection preparedness, and development of clinical trial strategies. Work setup: Travel up to 20%, based on project needs.