Medical Laboratory Director at CareDx

Waltham, MAFull-timeLABPosted about 2 months ago

About the Role

<div class="content-intro"> </div>CareDx is a leading precision medicine diagnostics company advancing care in transplant, specialty oncology, and cell therapy. Through our innovative portfolio of molecular diagnostics, digital health solutions, AI-powered data and analytics, and patient support services, we partner with healthcare providers, patients, and biopharma organizations to help inform clinical decision-making and improve patient outcomes. <div class="x_x_elementToProof">Within CareDx's Specialty Oncology business, we are focused on improving the management of HPV-driven cancers through innovative diagnostic solutions. NavDx®, our blood-based DNA test, helps clinicians detect molecular signs of disease recurrence, monitor treatment response, and guide patient management throughout the care journey. Our team is committed to expanding access to actionable insights that support more informed cancer care.</div> We are seeking a Medical Laboratory Director - CLIA Laboratory to provide clinical, scientific, regulatory, and administrative leadership for high-complexity CLIA laboratory operations. This Director-level role is responsible for ensuring the quality, accuracy, compliance, and timely delivery of laboratory testing services while supporting a culture of quality, collaboration, and continuous improvement. The Medical Laboratory Director will provide oversight of laboratory testing activities, interpretation of test results, consultation with physicians and other healthcare providers, and guidance to laboratory professionals. This leader will help ensure that laboratory results are accurate, reliable, and available in a timely manner to support patient care. This role will partner closely with Laboratory Operations and cross-functional stakeholders to support laboratory performance, quality assurance, regulatory compliance, staffing, budgeting, technology evaluation, and continuous process improvement. The position requires strong collaboration with laboratory operations, clinical, scientific, technical, regulatory, and corporate teams to advance company objectives and enhance patient care. Responsibilities:  <ul> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Provide clinical, scientific, regulatory, and administrative oversight for high-complexity CLIA laboratory testing services.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ensure laboratory operations and testing services comply with applicable regulatory and accreditation requirements, including CLIA, CAP, NY State CLEP, and other relevant regulatory bodies.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ensure testing systems, methodologies, and laboratory processes provide accurate, reliable, and high-quality results across the pre-analytic, analytic, and post-analytic phases of testing.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Provide clinical interpretation of laboratory test results and consultation to ordering physicians, patients, and other healthcare providers as appropriate.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Oversee quality assurance and quality control programs to monitor laboratory performance, identify quality issues, and support timely corrective and preventive actions.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ensure proficiency testing is performed in accordance with CLIA and other applicable requirements.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ensure acceptable levels of analytical performance are established and maintained for each test system.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ensure appropriate documentation of remedial actions when deviations from established performance specifications are identified, and ensure patient results are reported only when systems are functioning properly.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Maintain awareness of current and future laboratory accreditation standards and ensure duties are performed consistent with applicable regulatory expectations.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Participate in laboratory-related managerial decisions, including staff selection, test methods, equipment purchases, quality systems, safety, regulatory compliance, hours of operation, scheduling, and utilization management.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Partner with the head of Laboratory Operations on laboratory strategy, budgeting, resource planning, technology evaluation, and operational improvements.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Support the development, validation, and implementation of laboratory testing processes and methods in a high-complexity molecular diagnostics environment.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ensure the laboratory environment, physical plant, and safety conditions are appropriate for the testing performed and provide a safe work environment.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ensure approved procedure manuals are available to personnel responsible for all aspects of the testing process.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Lead, mentor, and support laboratory professionals, fostering a culture of quality, accountability, collaboration, high morale, and engagement.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Collaborate cross-functionally with laboratory, clinical, scientific, operations, technology, and corporate teams to support company objectives and patient care.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Establish and maintain effective communication with internal and external stakeholders to support laboratory service needs, clinical trends, and program planning.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Perform other responsibilities required by CLIA and other applicable local, state, federal, or accreditation requirements.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Required travel is <20%</li> </ul> Minimum Education, Experience, & Specialized Knowledge (Required):  Education and Certifications <ul> <li>M.D./D.O., and/or Ph.D. in a relevant scientific field such as chemistry, biology, clinical laboratory science, medical technology, or a related discipline.</li> <li>Eligible to hold valid Massachusetts, North Carolina, and California director licenses required.</li> <li>Qualification under the personnel regulations of the Clinical Laboratory Improvement Amendments of 1988 required.</li> <li>ABCC, ABMGG, and/or ABB certification strongly desired.</li> <li>Certification by the American Board of Pathology in Anatomic Pathology and/or Clinical Pathology preferred.</li> <li>ABP certification in Molecular Genetic Pathology preferred.</li> <li>Current Certificate of Qualification in Oncology, Molecular and Cellular Tumor Markers and eligible for Certificate of Qualification in Genetic Testing  issued by the New York State Department of Health</li> </ul> Experience <ul> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">At least 10 years of experience in a high-complexity CLIA laboratory focused on molecular diagnostics, including at least 5 years in a leadership role.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Demonstrated experience overseeing the scope, standards, and quality of clinical testing services.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Experience with all phases of developing, validating, and implementing high-complexity molecular testing in a CLIA environment.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Experience in molecular diagnostics, gene expression platforms, real-time PCR, and next-generation sequencing preferred.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Participation in clinical activities of multidisciplinary cancer care with the ability to communicate directly with treating physicians and patients.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Experience evaluating laboratory programs, solving complex problems, and building strong cross-functional relationships.</li> </ul> Knowledge, Skills, and Abilities <ul> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">In-depth knowledge of oncologic pathology, clinical laboratory operations, laboratory regulations, quality systems, and high-complexity molecular diagnostics.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Strong working knowledge of local, state, and federal laboratory regulations applicable to medical diagnostic testing.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Demonstrated ability to lead a diverse team of laboratory professionals and build a strong laboratory culture centered on quality, collaboration, engagement, and patient care.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Excellent interpersonal, communication, training, and relationship-building skills, with the ability to work effectively across multiple disciplines.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Highly organized, detail-oriented, and committed to strong documentation practices.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Results-oriented leader with strong integrity, sound judgment, and a commitment to quality.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ability to work effectively in a fast-paced, evolving corporate environment and adapt quickly to changing priorities.</li> <li style="font-family: 'times new roman', times, serif; font-size: 12pt;">Ability to collaborate cross-functionally with non-laboratory and non-scientific personnel to advance company objectives and enhance patient care.</li> </ul> CareDx, Inc. is an Equal Opportunity Employer-vets/disabled, and participates in the E-Verify program. By proceeding with our application and submitting your information, you acknowledge that you have read our <a href="https://nam04.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.caredx.com%2Fus-personnel-privacy-notice&data=05%7C02%7C%7C7909ec363e2b416b016a08de7886b61c%7C9ec77d4e480144b4b8fea5749eaf06b0%7C1%7C0%7C639080717137822026%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=rz649lSGHm5Ca8UOMhbSARMbRhbyMFHdOgEEBXImKs4%3D&reserved=0" target="_blank">U.S. Personnel Privacy Notice</a><a href="https://nam04.safelinks.protection.outlook.com/?url=http%3A%2F%2Fcaredx.com%2Fus-personnel-privacy-notice%2F&data=05%7C02%7C%7C82daf31a87e44746b2ea08dceef5e348%7C9ec77d4e480144b4b8fea5749eaf06b0%7C1%7C0%7C638647987067924758%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&sdata=fvNqQdyyA0YaWb3Y4bxHjbbzsxfJ4EmKAEMFQr39KnU%3D&reserved=0" target="_blank"> </a>and consent to receive email communication from CareDx. Certain jurisdictions require notice of how we use and protect your personal information. For more information, please read our <a href="https://caredx.com/privacy-center/#ca-privacy">Privacy Policy</a> The U.S. EEO posters are available <a class="HyperlinkV2 SCXO121329444 BCX8" href="http://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf" target="_blank">here</a>.  Note: We do not accept resumes from headhunters, placement agencies, or other suppliers that have not signed a formal agreement with us. <div class="content-pay-transparency"><div class="pay-input"><div class="description">This is the anticipated base salary range for candidates who will work in Waltham, MA. The final salary offered to a successful candidate will be dependent on several factors that may include, but are not limited to, the type and length of experience within the job, the type and length of experience within the 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. CareDx is a multi-state employer, and this salary range may not reflect positions that work in other states.</div><div class="title">United States</div><div class="pay-range">$142,000—$185,000 USD</div></div></div>

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