The Clinical Trial Associate (CTA) at Karius supports clinical research activities by assisting with the collection, quality control, and quality assurance of regulatory documents related to clinical trials. The role involves maintaining the Trial Master File (TMF), communicating with study teams and clinical sites, and ensuring compliance with regulatory standards. The CTA will also help with study documentation, tracking milestones, and coordinating meetings, all while building proficiency in clinical trial processes under guidance.
See how your résumé matches this role — and tailor it from what actually gets interviews.