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

Nurix Therapeutics · Brisbane, CA

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Role summary

Senior Clinical Trial Associate to independently manage trial master files, coordinate with CROs, and mentor junior staff at a clinical-stage biotech company. Lead TMF integrity, document development, and clinical supply coordination with minimal oversight.

What they're looking for

Bachelor's degree in science-related field or equivalent education and work experience
3–5+ years of clinical operations or clinical research experience
Demonstrated end-to-end ownership of TMF or vendor relationship management
Ability to resolve routine CRO and vendor issues independently
Experience mentoring or guiding junior team members
Strong verbal and written communication skills
Proficiency with MS Word, Excel, Outlook, and PowerPoint

What you'll be doing

Own study TMF plan development, tracking, and archiving of essential documents throughout trial lifecycle
Lead quality reviews of TMF and resolve discrepancies directly with CRO partners
Draft and finalize study documents including protocols, manuals, CRFs, and patient materials
Independently manage clinical supply and lab sample coordination, identifying risks proactively
Mentor junior CTAs and contribute to training materials and SOPs for the broader team

Compensation$134,500–$146,600 annually

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