Senior Clinical Trial Manager

Role: Clinical Trial Manager with 3-8 years of experience overseeing Phase I–III clinical trials, primarily in oncology. Responsibilities: manage study operations from start-up to closeout, develop timelines, coordinate CROs, vendors, and sites, monitor progress, ensure regulatory and GCP compliance, review documentation, oversee budgets, and support regulatory submissions. Qualifications: Bachelor's degree in Sciences, Nursing, Pharmacy, or related field; 3-5 years of clinical research experience; strong knowledge of ICH-GCP, trial systems (CTMS, EDC, eTMF); excellent project management and communication skills. HighValue: oncology, Phase I–III, vendor oversight, regulatory compliance, cross-functional collaboration, experience with external vendors and clinical systems. WorkSetup: not specified; typically office-based with potential local site visits.