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Senior Clinical Research Associate

Senior Clinical Research Associate

Precision Point StaffingSanta Rosa, CA, US
2 days ago
Job type
  • Full-time
Job description

Job Description

Senior Research Associate – Oncology

Location : San Francisco, CA (On-site 3 days / week)

Employment Type : Full-time

About the Opportunity

Our client, an innovative biotechnology company focused on advancing oncology therapeutics, is seeking a Senior Research Associate to join their clinical development team. This individual will play a key role in supporting oncology clinical studies and cross-functional research efforts from within the company’s San Francisco headquarters.

This is an on-site role (3 days per week) , offering the opportunity to collaborate closely with clinical operations, translational research, and biomarker teams in a highly interactive environment.

Key Responsibilities

  • Support the planning, execution, and monitoring of oncology clinical studies across multiple phases. (Phase II and III Preferred)
  • Collaborate cross-functionally with Clinical Operations, Data Management, Biometrics, and Translational Science to ensure study deliverables and timelines are met.
  • Assist with protocol review, study documentation, sample tracking, and data reconciliation activities.
  • Maintain study files and documentation in compliance with GCP and internal SOPs.
  • Contribute to internal study meetings, data reviews, and cross-team communications.
  • Manage and review laboratory samples and data from external partners and CROs.
  • Provide operational and scientific support for biomarker and translational research activities tied to ongoing clinical programs.

Required Qualifications

  • Bachelor’s or Master’s degree in Biology, Oncology, or a related life science field.
  • 3–6 years of relevant industry experience supporting oncology-focused clinical studies.
  • Proven track record contributing to clinical-stage oncology programs .
  • Solid understanding of clinical study workflows, GCP guidelines, and study documentation.
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