Startups · AI

Senior Clinical Trial Associate (Sr. CTA)

Nurix AI · Brisbane, California · On-site

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About Nurix AI

AI agents that run your enterprise workflows and get measurably better over time. 150+ enterprises live in production across retail, insurance, and financial services. Backed by Accel and General Catalyst.

About the role

You’ve done this before — now do it with more ownership. You’ll run the TMF for your studies end-to-end, work directly with CROs to resolve problems before they become problems, and help the CTAs around you get better at the job. You’ll independently own key operational pieces of our trials — from TMF integrity to vendor coordination — and mentor junior team members along the way.

What they're looking for

  • Own the study TMF plan end-to-end: development, tracking, and archiving of Essential Documents across the trial lifecycle
  • Lead quality reviews of the TMF and resolve discrepancies directly with the CRO
  • Draft and finalize study documents — plans, manuals, CRFs, and patient materials — with minimal oversight
  • Serve as a go-to resource for junior CTAs, providing informal mentorship and process guidance
  • Independently manage clinical supply and lab sample coordination, flagging risks before they escalate
  • Own data reconciliation issues across systems, looping in Data Management only when needed
More about this role

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

You’ve done this before — now do it with more ownership. You’ll run the TMF for your studies end-to-end, work directly with CROs to resolve problems before they become problems, and help the CTAs around you get better at the job.

You’ll independently own key operational pieces of our trials — from TMF integrity to vendor coordination — and mentor junior team members along the way.

  • Own the study TMF plan end-to-end: development, tracking, and archiving of Essential Documents across the trial lifecycle
  • Lead quality reviews of the TMF and resolve discrepancies directly with the CRO
  • Draft and finalize study documents — plans, manuals, CRFs, and patient materials — with minimal oversight
  • Serve as a go-to resource for junior CTAs, providing informal mentorship and process guidance
  • Independently manage clinical supply and lab sample coordination, flagging risks before they escalate
  • Own data reconciliation issues across systems, looping in Data Management only when needed
  • Represent Clinical Operations at portions of team meetings and Investigator Meetings
  • Help shape training materials and SOPs used across the broader CTA...

Read the full posting on Nurix AI's site ↗

Clinical Development & Safety

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