Clinical Research Associate
Confirmed live in the last 24 hours
Veracyte
Job Description
At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way – it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.
Our Values:
- We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
- We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work
- We Are Stronger Together: We collaborate openly, seek to understand, and celebrate our wins
- We Care Deeply: We embrace our differences, do the right thing, and encourage each other
The Position:
The Clinical Research Associate (CRA) – Lab Clinical Operations supports the execution of Veracyte’s clinical research programs, focusing on wet lab testing for clinical studies. This role ensures clinical samples are processed, tested, and reported in compliance with GCP, CLIA/CAP regulations, study protocols, and Veracyte SOPs.
Based at the San Francisco campus, the CRA partners with Clinical Affairs, Medical Affairs, and Laboratory Operations to ensure high-quality, compliant, and timely study execution.
Key Responsibilities
Clinical & Lab Operations
- Oversee sample receipt, tracking, processing, testing, and reporting for study-specific assays.
- Partner with the CLIA-certified laboratory to implement and monitor assay workflows.
- Ensure laboratory activities align with study protocols and regulatory requirements.
- Manage specimen lifecycle activities, including reconciliation and deviation resolution.
Study Management
- Support development and review of protocols, lab manuals, CRFs, and data plans.
- Assist with study start-up, site training, and laboratory readiness.
- Monitor laboratory data quality, turnaround times, and study metrics.
Cross-Functional Collaboration
- Work closely with Medical Affairs, Biostatistics, Data Management, Regulatory, QA, and Laboratory teams.
- Serve as the primary contact for laboratory-related inquiries from sites and internal stakeholders.
Who You Are:
- BS/BA in a scientific discipline required.
- 3–5 years of industry-sponsored clinical research experience including laboratory operations.
- Experience in oncology biomarkers or molecular diagnostics preferred.
- Working knowledge of GCP and CLIA/CAP laboratory environments.
- Strong organizational, communication, and cross-functional collaboration skills.
- Experience with CTMS, EDC, and/or LIMS systems preferred.
#LI-Onsite
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units.&l
