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 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. #J-18808-Ljbffr Kura Oncology, Inc.