Clinical Research Associate

<div class="content-intro"><p>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 <em>the Veracyte way</em> – 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. </p> <p>Our Values:</p> <ul> <li><strong>We Seek A Better Way</strong>: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care</li> <li><strong>We Make It Happen</strong>: We act with urgency, commit to quality, and bring fun to our hard work</li> <li><strong>We Are Stronger Together</strong>: We collaborate openly, seek to understand, and celebrate our wins</li> <li><strong>We Care Deeply</strong>: We embrace our differences, do the right thing, and encourage each other</li> </ul> <p> </p></div><h3><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">The Position:</span></h3> <p>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.</p> <p>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.</p> <h4> </h4> <h4>Key Responsibilities</h4> <h4>Clinical & Lab Operations</h4> <ul> <li>Oversee sample receipt, tracking, processing, testing, and reporting for study-specific assays.</li> <li>Partner with the CLIA-certified laboratory to implement and monitor assay workflows.</li> <li>Ensure laboratory activities align with study protocols and regulatory requirements.</li> <li>Manage specimen lifecycle activities, including reconciliation and deviation resolution.</li> </ul> <h4>Study Management</h4> <ul> <li>Support development and review of protocols, lab manuals, CRFs, and data plans.</li> <li>Assist with study start-up, site training, and laboratory readiness.</li> <li>Monitor laboratory data quality, turnaround times, and study metrics.</li> </ul> <h4>Cross-Functional Collaboration</h4> <ul> <li>Work closely with Medical Affairs, Biostatistics, Data Management, Regulatory, QA, and Laboratory teams.</li> <li>Serve as the primary contact for laboratory-related inquiries from sites and internal stakeholders.</li> </ul> <h3> </h3> <h3><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Who You Are:</span></h3> <ul> <li>BS/BA in a scientific discipline required.</li> <li>3–5 years of industry-sponsored clinical research experience including laboratory operations.</li> <li>Experience in oncology biomarkers or molecular diagnostics preferred.</li> <li>Working knowledge of GCP and CLIA/CAP laboratory environments.</li> <li>Strong organizational, communication, and cross-functional collaboration skills.</li> <li>Experience with CTMS, EDC, and/or LIMS systems preferred.</li> </ul> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"><span style="font-family: Helvetica, Arial, sans-serif; font-size: 14px;">#LI-Onsite</span></span></p> <p> </p> <p> </p><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p></p> <p class="x_MsoNormal"><span data-olk-copy-source="MessageBody">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.</span></p></div><div class="title">Pay range</div><div class="pay-range"><span>$110,000</span><span class="divider">—</span><span>$127,000 USD</span></div></div></div><div class="content-conclusion"><p> </p> <h3><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">What We Can Offer You</span></h3> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">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<sup>®</sup> in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.</span></p> <p> </p> <h3><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">About Veracyte</span></h3> <p>Veracyte (Nasdaq: VCYT) is a global diagnostics company whose vision is to transform cancer care for patients all over the world. We empower clinicians with the high-value insights they need to guide and assure patients at pivotal moments in the race to diagnose and treat cancer. Our Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. For more information, please visit <a href="https://cts.businesswire.com/ct/CT?id=smartlink&url=https%3A%2F%2Fwww.veracyte.com%2F&esheet=54340020&newsitemid=20251015446872&lan=en-US&anchor=www.veracyte.com&index=5&md5=4d48386b00ece1531372e2e593d7cd2d">www.veracyte.com</a> or follow us on <a href="https://cts.businesswire.com/ct/CT?id=smartlink&url=https%3A%2F%2Fwww.linkedin.com%2Fcompany%2Fveracyte%2F&esheet=54340020&newsitemid=20251015446872&lan=en-US&anchor=LinkedIn&index=6&md5=234cba826cb637f449d2722139f551ef">LinkedIn</a> or <a href="https://cts.businesswire.com/ct/CT?id=smartlink&url=https%3A%2F%2Fx.com%2Fveracyte%3Fs%3D11&esheet=54340020&newsitemid=20251015446872&lan=en-US&anchor=X+%28Twitter%29&index=7&md5=20ead95735af622bf261b20735515b66">X (Twitter)</a>.</p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our <a href="https://www.veracyte.com/privacy-statement-for-california-residents/" target="_blank">CCPA Disclosure Notice</a>.</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"><strong><span class="ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak">If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to <a class="fui-Link ___1rxvrpe f2hkw1w f3rmtva f1ewtqcl fyind8e f1k6fduh f1w7gpdv fk6fouc fjoy568 figsok6 f1hu3pq6 f11qmguv f19f4twv f1tyq0we f1g0x7ka fhxju0i f1qch9an f1cnd47f fqv5qza f1vmzxwi f1o700av f13mvf36 f1cmlufx f9n3di6 f1ids18y f1tx3yz7 f1deo86v f1eh06m1 f1iescvh fhgqx19 f1olyrje f1p93eir f1nev41a f1h8hb77 f1lqvz6u f10aw75t fsle3fq f17ae5zn" href="mailto:careers@Veracyte.com" target="_blank">careers@veracyte.com</a></span></strong></span></p></div>