Clinical Trial Associate (CTA) NX-5948-203

Role: Support clinical trial operations as a Clinical Trial Associate, focusing on documentation, data management, and trial logistics. Responsibilities: assist with study document creation (plans, CRFs, manuals), manage TMF documentation and quality reviews, coordinate clinical supplies and lab logistics, support data review and reporting, help prepare training materials, and facilitate meeting coordination. Requirements: Bachelor’s degree in a science-related field; 0-2 years of clinical operations or research experience; strong attention to detail; excellent communication skills; proficiency with MS Office. Preferred: exposure to electronic TMF systems. High-Value: Entry-level role supporting biopharma clinical trials in a collaborative, solutions-oriented environment. Location: onsite in Brisbane, CA.