Veracyte

Clinical Research Associate

Veracyte$110K — $127K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA in a scientific discipline required.
  • 3-5 years of experience in medical research, laboratory, histology, IVD, nursing, or biopharmaceutical industry.
  • Minimum 2 years of laboratory experience, including specimen processing and molecular assay testing.
  • Preferred experience in clinical trial operations, data management, site management, or regulatory coordination.
  • Working knowledge of GCP and CLIA/CAP laboratory environments.
  • Experience in oncology biomarkers or molecular diagnostics preferred.
  • Familiarity with CTMS, EDC, and/or LIMS systems preferred.

Responsibilities

  • Oversee sample receipt, tracking, processing, testing, and reporting for study-specific assays.
  • Partner with R&D and CLIA-certified laboratory to implement, conduct, and monitor assay workflows.
  • Ensure laboratory activities align with study protocols and regulatory requirements.
  • Manage specimen lifecycle activities, including reconciliation and deviation resolution.
  • 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.

Benefits

  • Competitive compensation and benefits package.
  • Significant career opportunities within a growing company.
  • Commitment to fostering an inclusive workforce.
  • Recognition as a Great Place to Work in both the US and Israel.
  • Engagement in innovative ideas and decisions.
Full Job Description
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, R&D, 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 R&D and CLIA-certified laboratory to implement, conduct, 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 R&D, 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 experience in medical research, laboratory, histology, IVD, nursing, or the biopharmaceutical industry
  • Minimum 2 years of laboratory experience, including specimen processing and molecular assay testing
  • Experience in clinical trial operations, data management, site management, or regulatory coordination preferred
  • Working knowledge of GCP and CLIA/CAP laboratory environments
  • Experience in oncology biomarkers or molecular diagnostics preferred
  • Familiarity with CTMS, EDC, and/or LIMS systems preferred
  • Strong organizational, communication, and cross-functional collaboration skills

#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.

Pay range

$110,000-$127,000 USD

What We Can Offer You

Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.

About Veracyte

Veracyte is a genomic diagnostics company that uses advanced genomic technology to resolve diagnostic uncertainty and deliver actionable results that improve patient care and outcomes. The company's tests in thyroid, lung, and breast cancer, and in idiopathic pulmonary fibrosis, are becoming standard of care in helping patients avoid unnecessary invasive procedures, while resolving inconclusive results from traditional diagnostic methods. Veracyte's genomic tests are covered by Medicare and many commercial insurance plans. With Veracyte's exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide. The company was founded in 2008 and is headquartered in South San Francisco, California.
Learn more about Veracyte
Size
761 employees
Market Cap
$1.8 billion
Industry
Net Income
-$34.9 million
Founded
2006
5 Year Trend
+27.5%
Revenue
$117.4 million
NASDAQ

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