Senior CTA: TMF Lead & End-to-End Ops Mentor

RiseMe; Brisbane (CA); On-site; USD 135,000 - 147,000; Full time

Job summary

Nurix Therapeutics in Brisbane, CA is seeking a Senior Clinical Trial Associate (Sr. CTA) to own TMF integrity, coordinate CRO activities, and guide junior CTAs. You’ll draft study documents, manage trial logistics, and address issues before they impact timelines.

This hands-on role requires strong communication, problem-solving, and a collaborative mindset. You’ll work onsite with cross-functional teams, support training materials, and help ensure regulatory readiness across studies while

Qualifications

• Bachelor's degree (BS/BA) or equivalent in a science-related field.
• 3–5+ years of Clinical Operations or clinical research experience.
• Demonstrated ownership of a TMF or vendor relationship from start to finish.
• Comfortable resolving routine CRO/vendor issues independently before escalating.
• Experience mentoring or guiding junior team members.
• Excellent verbal and written communication skills.
• Proficiency with MS Word, Excel, Outlook, and PowerPoint.

Responsibilities

• Own 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 with the CRO.
• Draft and finalize study documents — plans, manuals, CRFs, and patient materials — with minimal oversight.
• Mentor junior CTAs and provide process guidance.
• Coordinate clinical supply and lab sample handling, flag risks early.
• Resolve data reconciliation issues across systems; involve Data Management when needed.
• Represent Clinical Operations at team meetings and Investigator Meetings.
• Contribute to training materials and SOPs used across the CTA team.

Skills

Clinical Operations

TMF ownership

Mentoring

Communication

MS Office

Education

Bachelor's degree in science

Tools

MS Word

Excel

Outlook

PowerPoint

Job description

Nurix Therapeutics in Brisbane, CA is seeking a Senior Clinical Trial Associate (Sr. CTA) to own TMF integrity, coordinate CRO activities, and guide junior CTAs. You’ll draft study documents, manage trial logistics, and address issues before they impact timelines.

This hands-on role requires strong communication, problem-solving, and a collaborative mindset. You’ll work onsite with cross-functional teams, support training materials, and help ensure regulatory readiness across studies while