CLIA Lab Director
Valius overview
At Valius, we believe that the future of cancer care will be defined by “maximalist” diagnostics: deep, comprehensive assessments of DNA, RNA, and protein designed to give patients and their care teams the best possible understanding of how their tumor works and what its vulnerabilities are.
We’re building the diagnostics and bioinformatics company to power this future, starting by applying this approach to patients with challenging cancers. In our first year, we worked with over 75 of these patients and, in many cases, identified plausible therapeutic targets which had not been discovered previously. This coming year, we’re on track to scale our patient volume significantly, all while bringing new diagnostic modalities (e.g., single-cell transcriptomics) and analytical approaches into clinical care for the very first time.
We’ve just raised a $13.5M seed round, led by 8VC and Basis Set Ventures, and are looking for people passionate about changing cancer care to join our growing team.
CLIA Lab Director role
We're hiring a Lab Director to join our team in San Francisco to lead the buildout and operation of Valius's first clinical laboratory. This is a foundational role at a company at the intersection of cancer biology, multi-omic profiling, and precision medicine. You'll own the design, accreditation, and day-to-day operations of our CLIA/CAP-certified lab, establishing the infrastructure that will enable delivery of high-complexity molecular diagnostics directly to our cancer patients and their care teams. This is a rare opportunity to build something from the ground up in a mission-driven environment.
This is an in-person role in either San Francisco or Boston.
What you’ll do
Lab design and buildout
Lead the end-to-end design, buildout, and commissioning of Valius's CLIA laboratory, from physical space planning through instrument installation and workflow validation
Define lab infrastructure requirements including equipment, consumables, LIMS, and workflow automation to support clinical-grade reproducibility and scale
Establish and document standard operating procedures (SOPs), quality management systems (QMS), and training programs from the ground up
Accreditation and compliance
Prepare and manage all aspects of laboratory accreditation, including CAP inspection readiness, CLIA certification, and New York State approval
Serve as the CLIA Laboratory Director of record, taking responsibility for all aspects of laboratory compliance across pre-analytic, analytic, and post-analytic phases
Laboratory operations
Direct day-to-day clinical lab operations, ensuring timely, accurate, and compliant processing of patient samples and reporting of results
Oversee implementation and validation of complex molecular assays, including 10x Genomics next-generation single-cell and spatial RNA sequencing
Manage technical transfer of assays from R&D into clinical operations
Implement metrics for assay performance, turnaround time, and quality
Team and cross-functional leadership
Recruit, train, and lead a team of clinical laboratory scientists, supervisors, and technologists; conduct competency assessments in line with CLIA requirements
Collaborate closely with computational biologists and translational scientists to integrate lab outputs into patient-facing reports
Partner with bioinformatics and operations teams to ensure data integrity and compliant reporting of high-complexity results
Contribute to scientific and operational strategy as a senior leader within Valius
What you’ll bring
Advanced degree (PhD, MD, or MD/PhD) in a relevant scientific discipline (molecular biology, genomics, clinical laboratory science, or related field)
Eligibility to serve as a High-Complexity Laboratory Director under CLIA regulations (HCLD board certification, or an MD/PhD with the required training and experience per 42 CFR Part 493)
Minimum 8-10 years of experience in clinical laboratory operations, with at least 5 years in a leadership or director-level role overseeing a CAP/CLIA-certified laboratory
Proven track record of successfully establishing or scaling a clinical lab
Expert-level experience implementing and validating advanced molecular diagnostic assays such as bulk RNA sequencing, whole exome sequencing, and/or single-cell RNA sequencing using a 10x Genomics platform
Deep working knowledge of quality systems, documentation control, and regulatory requirements for LDTs, including SOPs, CAPA processes, and proficiency testing programs
Experience with LIMS platforms, electronic quality management systems (eQMS), and workflow automation in a high-complexity testing environment
Strong ability to recruit, develop, and retain scientific staff
Excellent written and verbal communication skills; ability to translate complex laboratory data into clear, actionable information for clinical, scientific, and executive stakeholders
Commitment to our patient-focused mission
Interest in working for a small, early-stage startup
What we’ll bring
Competitive salary and equity compensation
Generous refresh grants
Comprehensive benefits (health, dental, vision, 401(k))
Genuine investment in your professional development
Fun, mission-driven team culture