About this opportunity
Nurix Therapeutics lists this Senior Clinical Trial Associate (Sr. CTA) NX-1607 opportunity in brisbane, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Role
Manage key operational aspects of clinical trials, including TMF integrity, vendor coordination, and study document management, while mentoring junior team members.
Responsibilities
develop, track, and archive essential trial documents;
lead TMF quality reviews and resolve discrepancies with CROs;
independently draft study plans, manuals, and patient materials;
coordinate clinical supplies and lab samples;
manage data reconciliation issues;
represent Clinical Operations in meetings and contribute to training material development.
Requirements
Bachelor's degree or equivalent;
3–5+ years in Clinical Operations or clinical research;
proven ownership of TMF and vendor relationships;
strong problem-solving and communication skills;
proficiency in MS Office.
Preferred qualifications
Preferred qualifications are not specified.
High-Value
role involves CRO/vendor oversight, study document management, and operational problem resolution within a biopharma clinical trial setting.
Location
onsite in Brisbane, CA.
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Worksite address
brisbane, CA, 94005, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.