CLIA Laboratory Director (Part-time / Consultant)

Your Responsibilities:

• Act as Part-time/Consultant Laboratory Director for ProtaGene’s two CLIA high-complexity laboratories in Burlington,Massachusetts, USA and Heidelberg, Germany, in accordance with 42 CFR §§ and .
• Ensure both laboratories operate in compliance with applicable CLIA, CAP, and relevant state requirements, includingMassachusetts, California, and Pennsylvania requirements; New York State qualification considered an asset.
• Review and approve relevant test methods, validation activities, procedures, report formats, and major changes affectingclinical testing.
• Oversee the suitability, training, competency, and delegated responsibilities of laboratory personnel involved in high complexity testing.
• Conduct a minimum of two on-site oversight visits per calendar year to each laboratory location (Burlington and Heidelberg),with travel costs covered separately.
• Review quality-control, proficiency testing/alternative assessment, and performance data; ensure appropriate action is takenwhere issues are identified.
• Provide scientific and clinical consultation on complex technical, quality, reporting, or compliance matters.
• Support regulatory inspections, CAP/CLIA activities, licence applications, and customer audits as needed.
• Participate in scheduled oversight meetings and site visits, and remain available for significant quality, regulatory, or patient impact events.
• Maintain appropriate documentation of oversight, reviews, decisions, and delegated responsibilities.
• Contribute to and comply with corporate safety, environmental, and quality standards.

Note: The Laboratory Director retains independent professional authority and accountability for the quality, reliability, andregulatory compliance of testing performed under each laboratory’s CLIA certificate.

Note: While the ideal candidate shall be available for both ProtaGene laboratories, those capable of holding only one of the twosites may also be considered.

We Offer:

• This is a part-time consulting role requiring a commitment of 12 consulting hours per month across both laboratories.
• A minimum of 12 hours of consulting work per month at a rate of $500/hr for a minimum monthly total of $6000.
• Two paid visits to the company’s site in Heidelberg, Germany, per year, with travel time and reasonable travel expenses compensated separately.
• Two paid visits to the company’s site in Burlington, MA, USA, per year, with travel time and reasonable travel expenses compensated separately.
• Work for a dynamic, innovative company that values appreciation, openness and respect as well as a lively feedback culture.

Your Qualifications:

• Eligible to serve as Clinical Laboratory Director for two CLIA laboratories performing high-complexity testing, in accordance with 42 CFR § , 105 CMR 180.060, and any applicable requirements for California and Pennsylvania laboratory licensure.
• Meet the applicable Massachusetts and CLIA director-qualification pathway, including either:
  • MD or DO licensed to practise in Massachusetts and board-certified in anatomic and/or clinical pathology; or
  • Earned doctoral degree in a chemical, biological, clinical, or medical laboratory science, medical technology, molecular
    biology, genetics, genomics, or a closely related discipline, together with certification by an HHS-approved andMassachusetts-acceptable specialty board.
  • For non-physician candidates, at least two years of laboratory training and/or experience and at least two years’experience directing or supervising high-complexity testing in the relevant specialty.
• Board certification in clinical molecular genetics/genomics or a directly relevant specialty is required or strongly preferred,depending on the candidate’s CLIA qualification pathway (e.g., ABMGG or another HHS-approved board).
• Demonstrated experience in clinical molecular diagnostics, genomics, NGS and/or other high-complexity genetic testingrelevant to the laboratory’s test menu.
• Strong working knowledge of CLIA, CAP accreditation, Massachusetts clinical laboratory requirements, method validation/verification, proficiency testing or alternative assessment, personnel competency, quality control, and clinical reporting.
• Ability to meet additional laboratory-director, technical-director, or state qualification requirements for jurisdictions in whichthe laboratory holds, or intends to obtain, licences or permits. A minimum of California and Pennsylvania is required.
• Integrity, commitment, and a motivated work ethic.
• Ability to work in a team and independently.
• Strong organizational and interpersonal skills.
• Ability to troubleshoot, solve difficult problems, and propose solutions relating to laboratory organization and management.
• Self-motivated, curious and results oriented with minimal oversight.
• Effective collaborator with internal and external partners to develop and maintain the overall strategies.
• Excellent written and verbal communication skills, ability to work well with colleagues from diverse backgrounds and cultures.