Precision Point Staffing
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 companys 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 Bachelors or Masters degree
in Biology, Oncology, or a related life science field. 36 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.
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 companys 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 Bachelors or Masters degree
in Biology, Oncology, or a related life science field. 36 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.