Clinical Trial Associate

Role: Clinical Trial Associate supporting operational execution of oncology clinical trials across all phases, ensuring compliance, milestone achievement, and efficient study conduct. Responsibilities: coordinate trial start-up, monitoring, close-out activities, manage vendor and site documentation, oversee TMF compliance using eTMF systems, track study metrics, and support inspection readiness. Collaborate with internal teams, CROs, and vendors; assist with study documentation, site monitoring, and regulatory compliance. Qualifications: bachelor’s in a scientific field, 1-2 years of clinical research experience or equivalent; strong organizational, communication, and documentation skills; familiarity with GCP, FDA regulations, and eTMF systems (e.g., Veeva Vault). Preferred: experience in oncology, CRO oversight, and working in high-volume environments. HighValue: oncology trials, clinical operations, GCP compliance, CRO/vendor oversight, eTMF management, minimal travel. WorkSetup: primarily office-based with potential for some travel.