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We are seeking an experienced and highly skilled Molecular Genetics Clinical Laboratory Director – Oncology or Senior Laboratory Director – Oncology to provide technical leadership and oversee the daily operations of our high-complexity oncology clinical laboratory. The Oncology Laboratory Director is responsible for ensuring accurate interpretation and reporting of oncology test results, maintaining regulatory compliance, driving quality improvements, and collaborating cross-functionally to advance our oncology assays.
Job Responsibility:
Provide technical oversight to ensure high-quality oncology testing and alignment with laboratory and clinical goals
Interpret somatic variant results from Northstar liquid biopsy assays, classify variants, and sign out oncology clinical reports
Troubleshoot technical issues related to oncology workflows, including liquid biopsy sample prep, NGS library preparation, sequencing, and data analysis
Evaluate lab performance, implement process improvements, and promote robust quality assurance systems
Review Non-Conforming Events and CAPAs to ensure timely resolution of issues impacting oncology test performance
Ensure compliance with CLIA, CAP, NYSDOH, and other applicable regulatory standards for oncology assays
Oversee accurate documentation of SOPs, validation reports, QC records, personnel competencies, proficiency testing, and report archives
Collaborate with bioinformatics, R&D, and medical affairs on assay development, interpretation guidelines, and continuous assay optimization
Participate in budget planning and manage lab expenses to ensure financial efficiency while maintaining exceptional quality
Support special projects, including scaling new oncology tests, preparing for inspections, and implementing automation
Serve as a subject matter expert on oncology variant interpretation, including AMP/CAP/NYS guidelines
Requirements:
Doctoral degree (PhD, MD, or equivalent) in genetics, molecular biology, or a related field
Board certification (ABMGG, ABP in Molecular Genetic Pathology, or equivalent)
Valid or eligible for California Clinical Laboratory Director license (CGMB, CGMBS, MD/DO licensure) and New York State CoQ in oncology testing
4+ years in a regulated clinical laboratory environment (CLIA/CAP/NYSDOH), with at least 3 years in molecular oncology testing including NGS
Proven leadership in developing, validating, and implementing oncology assays (e.g., somatic mutation panels, methylation assays)
Deep knowledge of cancer genomics, including tumor heterogeneity, somatic driver mutations, and targeted therapies
Experience with variant interpretation databases (COSMIC, OncoKB, ClinVar), IGV, BAM file review, and molecular tumor board participation
Strong analytical, communication, and organizational skills, with a track record of leading teams in high-growth environments
Proficiency with LIMS and oncology-focused bioinformatics tools
What we offer:
Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)
Free daily on-site lunches provided from top eateries
A variety of perks on campus (state of the art gym, restaurant)
Free on-site EV charging (compatible with all EVs, including Tesla)
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