Clinical Trial Associate

Role: Clinical Trial Associate supporting Clinical Operations, focused on trial administration and documentation management. Responsibilities: develop study tools, track study documents and approvals, manage contracts and budgets, facilitate site identification and insurance processes, assist with eTMF setup and filing, coordinate study training, support trial registration, organize meetings, and contribute to SOP improvements. Requirements: strong organizational skills, multitasking ability, effective communication, proficiency in MS Office and Veeva eTMF, understanding of GxP and ICH-GCP, with a focus on documentation accuracy. Preferred: 1+ year relevant experience or a 4-year college degree. High-Value: biopharma, clinical trials, GxP compliance, eTMF management, cross-functional cooperation, supporting studies in the development pipeline. Work Setup: location not specified but involves collaborative tasks and document management.