Senior Clinical Trial Associate (Sr. CTA) NX-1607

Role: Manage key operational aspects of clinical trials, including TMF integrity, vendor coordination, and study document management, while mentoring junior team members. Responsibilities: develop, track, and archive essential trial documents; lead TMF quality reviews and resolve discrepancies with CROs; independently draft study plans, manuals, and patient materials; coordinate clinical supplies and lab samples; manage data reconciliation issues; represent Clinical Operations in meetings and contribute to training material development. Requirements: Bachelor's degree or equivalent; 3–5+ years in Clinical Operations or clinical research; proven ownership of TMF and vendor relationships; strong problem-solving and communication skills; proficiency in MS Office. Preferred qualifications are not specified. High-Value: role involves CRO/vendor oversight, study document management, and operational problem resolution within a biopharma clinical trial setting. Location: onsite in Brisbane, CA.