Clinical Trial Associate (CTA) NX-5948-203
Nurix•Brisbane, CA
•Onsite
About The Position
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. 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.
Requirements
- 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
- Sharp attention to detail — you catch what others miss
- Excellent verbal and written communication skills
- Proficiency with MS Word, Excel, Outlook, and PowerPoint
Nice To Haves
- Exposure to or coursework involving electronic Trial Master File systems is a plus
Responsibilities
- 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
Benefits
- Strong team orientation; highly collaborative
- Solutions and results-oriented focus
- Hands-on approach; resourceful and open to diverse points of view
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
