FRACTIONAL CLIA LABORATORY DIRECTOR - Molecular Boarded MD, Pathology or ABMGG Board-Certified PhD

Job Description

NOW HIRING: FRACTIONAL CLIA LABORATORY DIRECTOR - Molecular Boarded MD, Pathology or ABMGG Board-Certified PhD - Must have prior Fractional CLIA Laboratory Director for start up experience!!!

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Location: Washington, DC

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Schedule: 1 Day Per Week – Onsite

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Position Type: Fractional / Part-Time / Consulting

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Company: Start-Up Research Organization-Pending FDA Clearance

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Recruitment Firm: Staff Icons, LLC – Pathologist Recruitment Division

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See Job Description below:

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Interested in Learning More?

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If you are a board-certified Molecular Pathologist or ABMGG-certified PhD scientist interested in a flexible, fractional CLIA Laboratory Director opportunity in Washington, DC, we welcome a confidential conversation.Please forward your CV and contact information to:

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Staff Icons, LLC – Pathologist Recruitment Division

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Email: View email address on ziprecruiter.com

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Phone: View phone number on ziprecruiter.com

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Website:

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Exciting Leadership Opportunity!

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Staff Icons is seeking an experienced Fractional CLIA Laboratory Director for an innovative start-up research organization located in Washington, DC.

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The company is actively working toward obtaining FDA clearance or approval for its technology and is seeking an experienced laboratory leader to provide scientific expertise, regulatory guidance, and laboratory oversight during this important phase of development.

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This is an exciting opportunity for a board-certified Molecular Pathologist or an American Board of Medical Genetics and Genomics (ABMGG) board-certified PhD scientist to become involved with an emerging organization advancing innovative molecular technologies.

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The position requires an onsite commitment of just one day per week , offering flexibility while playing an important role in establishing laboratory quality, regulatory compliance, and operational readiness.

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Key Responsibilities

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• Serve as the designated CLIA Laboratory Director, subject to applicable regulatory qualifications and approval.
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• Provide leadership and oversight of laboratory operations, quality assurance, and regulatory compliance.
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• Support the organization's efforts toward FDA clearance or approval by collaborating with scientific, regulatory, and executive leadership.
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• Provide guidance on laboratory testing procedures, analytical validation, documentation, and quality systems relevant to regulatory submissions.
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• Ensure laboratory policies and procedures meet applicable CLIA requirements.
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• Oversee molecular testing methodologies, test validation, verification, and quality control activities as applicable.
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• Assist with establishing and maintaining standard operating procedures (SOPs).
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• Support laboratory inspection readiness, accreditation preparation, and regulatory documentation.
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• Provide oversight of laboratory personnel qualifications, training, and competency assessments as applicable.
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• Collaborate with the company's research and development teams to support scientific innovation and future clinical applications.
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Required Qualifications

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• MD, DO, or PhD from an accredited institution.
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• Board certification in Molecular Genetic Pathology or an applicable American Board of Medical Genetics and Genomics (ABMGG) specialty.
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• Expertise in molecular pathology, molecular genetics, or molecular diagnostic testing.
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• Experience with CLIA laboratory regulations, quality management, and regulatory compliance.
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• Ability to meet applicable CLIA Laboratory Director qualifications.
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• Strong leadership, communication, and organizational skills.
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• Availability to work onsite in Washington, DC, one day per week.
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Preferred Qualifications

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• Previous experience serving as a CLIA Laboratory Director or Medical Director.
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• Experience with FDA-regulated diagnostic products, FDA clearance or approval processes, or regulatory submissions.
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• Knowledge of molecular diagnostics, next-generation sequencing (NGS), genomic testing, or related technologies.
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• Familiarity with CAP accreditation and laboratory inspections.
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• Experience supporting start-up laboratories, biotechnology organizations, or research and development initiatives.
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• Experience with analytical validation, laboratory quality systems, and regulatory readiness.
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Why Consider This Opportunity?

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• Flexible Schedule: Only one onsite day per week.
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• Innovative Start-Up: Join an emerging research organization advancing molecular technologies.
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• FDA Regulatory Milestone: Contribute to a company actively pursuing FDA clearance or approval.
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• Leadership Opportunity: Help establish the scientific, operational, and regulatory foundation of a growing organization.
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• Professional Flexibility: Ideal for an experienced Molecular Pathologist or ABMGG-certified PhD scientist seeking a fractional leadership engagement.
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• Meaningful Impact: Play an important role in supporting the company's scientific development and future commercialization goals.
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Connecting exceptional laboratory leaders with innovative organizations nationwide.

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