Clinical Trial Associate (CTA) NX-5948-203

Clinical Trial Associate (CTA) NX-203 This is where a clinical operations career starts. You’ll learn the mechanics of running a trial — TMF management, document coordination, vendor touchpoints — with an experienced team showing you how it’s done, on studies that matter. Position Description You’ll support Clinical Operations across every phase of our trials, working closely with the study team to keep documents, data, and timelines on track. The Opportunity Help build and maintain study documents — plans, CRFs, manuals, and patient-facing materials Support the study TMF plan: track, collect, and file Essential Documents under the guidance of senior team members Assist with quality reviews of the TMF, flagging discrepancies for CRO follow-up Coordinate clinical supplies and lab sample logistics Support review of clinical data, listings, and reports Help build training materials and keep study trackers/metrics current Support meeting logistics — agendas, minutes, and Investigator Meeting coordination Take on additional projects as you grow into the role What You’ll Bring Bachelor’s degree (BS/BA) or equivalent combination of education and work experience in a science-related field 0–2 years of Clinical Operations or clinical research-related experience Exposure to or coursework involving electronic Trial Master File systems is a plus Sharp attention to detail — you catch what others miss Excellent verbal and written communication skills Proficiency with MS Word, Excel, Outlook, and PowerPoint Salary Range: $111,800 – $123,000 annually The posted range applies to roles based in the San Francisco Bay Area and reflects local market conditions. Where an offer lands within that range depends on the candidate’s relevant experience, technical expertise, and how their background aligns with the role’s requirements. Location: Onsite - Brisbane, CA Fit with Nurix Culture and Values Strong team orientation; highly collaborative Solutions and results-oriented focus Hands-on app