Clinical Trial Associate (CTA) NX-5948-203

NurixNurixBrisbane, California, United States
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Posted

9/24/2026

Employment

Full time

Range

$112k - $123k/year

Work style

On-site

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AI summary

Core responsibilities

The Clinical Trial Associate will support clinical operations by managing study documents, tracking timelines, and coordinating vendor and site logistics. They will also assist with TMF quality reviews, clinical data reporting, and meeting coordination to ensure study compliance.

Requirements overview

Candidates must possess a Bachelor's degree in a science-related field and have 0-2 years of experience in clinical operations or research. Proficiency in MS Office and strong attention to detail are required for this role.

Key skills

TMF managementDocument coordinationClinical operationsClinical researchData managementQuality reviewClinical supplies logisticsLab sample logisticsMeeting coordinationMS WordMS ExcelMS OutlookMS PowerPointAttention to detailCommunication skills

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Education requirements

bachelor degree

About Nurix

Industry

Biotechnology

Employees

379

Type

Public Company

Size

201-500 employees

Important Notice to Candidates: Nurix representatives with never conduct interviews by text and will never request personal financial information or ask candidates to purchase equipment. At Nurix Therapeutics, we aim to fundamentally change the way disease is treated using degrader-based medicines. Our journey began with a vision to harness the power of the cell’s natural protein degradation machinery, the ubiquitin-proteasome system, to create a new class of therapeutics that can overcome the limitations of current treatments.

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Job categories

HealthcareScience & ResearchAdministrative

Description

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 approach; resourceful and open to diverse points of view About Nurix Therapeutics Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.

Requirements

  • •TMF management
  • •Document coordination
  • •Clinical operations
  • •Clinical research
  • •Data management
  • •Quality review
  • •Clinical supplies logistics
  • •Lab sample logistics
  • •Meeting coordination
  • •MS Word
  • •MS Excel
  • •MS Outlook
  • •MS PowerPoint
  • •Attention to detail
  • •Communication skills

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