Temp Research Associate, Translational Medicine

About the Position

Temp Research Associate, Translational Medicine

We’re seeking a Research Associate, Translational Medicine for our well-known client based in Redwood City, CA. The selected candidate will play a key role in supporting Translational Medicine by developing and implementing biomarker and/or Companion Diagnostic (CDx) strategies for RAS(ON) inhibitor clinical trials. This position offers the opportunity to work in a collaborative and innovative environment while contributing to multiple ongoing clinical studies.

Responsibilities

• Partner with CDx Leads, Clinical Biomarker Leads, Biomarker Scientists, and broader Translational Medicine team members to support the execution of CDx and biomarker strategies, including clinical trial sample testing.
• Perform detailed reviews of clinically relevant documents to ensure data accuracy, integrity, and compliance with study protocols for RAS(ON) inhibitor clinical trials.
• Conduct data review, reconciliation, and quality control for genomic and biomarker data generated in clinical studies, ensuring accuracy, completeness, and alignment with source records, laboratory outputs, and protocol requirements.

Requirements

• Bachelors or Masters degree in cancer biology, cell or molecular biology, or a related field.
• Minimum of 1 year of relevant experience with an MS degree or 3 years with a BS degree in a biotech, pharmaceutical, or IVD diagnostic company.
• Strong coordination skills with cross-functional study teams and CRO partners.
• Excellent organizational skills, strong attention to detail, and effective time management with the ability to adapt to shifting priorities.
• Strong written and verbal communication skills.
• Proficiency in quality control of scientific data.
• Ability to thrive in detail-oriented work within fast-paced, team-based environments.

Nice to Have

• Knowledge or experience in oncology drug development and precision medicine.
• Familiarity with clinically relevant biomarker technologies across platforms such as NGS and qPCR/ddPCR.
• Understanding of clinical trial design and biomarker integration.
• Understanding of CDx development and regulatory requirements (e.g., FDA, EU-IVDR).

We Offer

Full-time employees are also eligible for benefits options such as health coverage, life insurance, disability insurance, and 401k benefits.

About the Company

At Advanced Clinical, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. Advanced Clinical is committed to providing employment opportunities without regard to sex, race, color, age, national origin, religion, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.

Advanced Clinical complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities. If a reasonable accommodation is needed to participate in the job application or interview process, please contact [email protected].