Clinical Laboratory Supervisor

ALMAC Group; Durham (NC); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical, Vision & Dental benefits

20 days PTO per year

401k company contribution

Job summary

ALMAC Group in Durham is seeking a Clinical Laboratory Supervisor to manage daily clinical testing activities. Responsibilities include supervising staff and ensuring compliance with regulatory standards in a fast-paced, high-complexity laboratory.

The ideal candidate has a B.S. or M.S. in a related field or a Ph.D., with experience in qPCR, Nanostring, and/or NGS technologies. Competitive benefits include medical coverage, PTO, and professional development opportunities.

Qualifications

• B.S. degree with 4+ years of training/experience in qPCR, Nanostring or NGS.
• Ph.D. with 1+ year of training/experience in qPCR, Nanostring or NGS.
• Experience in a high complexity CLIA testing environment.

Responsibilities

• Supervise testing personnel in high-complexity Clinical Testing Laboratory.
• Coordinate activities of junior team members for timely completion of testing.
• Monitor specimen examinations to maintain acceptable analytic performance.

Skills

qPCR

Nanostring

NGS

Communication skills

Attention to detail

Education

B.S. in chemical, biological, medical, clinical laboratory science, or medical technology

M.S. in relevant field

Ph.D. in relevant field

Job description

Clinical Laboratory Supervisor

The Clinical Laboratory Supervisor is responsible for overseeing the day‑to‑day testing activities in the Diagnostic Services' CLIA accredited Clinical Testing Laboratory. This includes supervision of high complexity molecular testing within global clinical trials, management of scientific staff and accurate reporting of test results across a wide range of technology areas. The post holder will drive continuous improvement and support a culture of scientific integrity and patient care.

As a key leader within Almac Diagnostic Services, the Clinical Laboratory Supervisor drives operational excellence and innovation in a fast‑paced, high‑complexity clinical laboratory. This role is responsible for supervising and mentoring a talented team, ensuring the highest standards in molecular diagnostic testing, and maintaining rigorous compliance with regulatory and quality standards. The Supervisor will play a pivotal role in advancing clinical trial outcomes, optimizing laboratory workflows, and fostering a culture of continuous improvement and professional development. This is an exciting opportunity for a motivated professional to make a significant impact on patient care and contribute to the advancement of precision medicine.

SHIFT Sun-Wed or Wed-Sat

Responsibilities

• Provide day‑to‑day supervision of testing personnel and reporting of test results within the high‑complexity Clinical Testing Laboratory
• Coordinate the activities of junior team members to ensure the completion of clinical testing within agreed timeframes
• Monitor specimen examinations and test analyses to ensure that acceptable levels of analytic performance are maintained at all times.
• Responsible for the generation, revision, and/or review of laboratory or equipment‑related SOPs and other quality documents
• Perform molecular biological techniques adhering to the laboratory's quality control policies
• Ensure that all remedial actions are taken in a timely manner whenever test systems deviate from the laboratory's established performance specifications and leadership is notified as required
• Be accessible to testing personnel at all times testing is performed to provide on‑site, telephone or electronic consultation to resolve technical problems in accordance with policies and procedures
• Monitor batch manufacturing stock levels and coordinate ordering and testing of new reagent and control batches to ensure adequate supply for clinical testing. Verify reagents, consumables, and laboratory equipment are qualified for use and within expiry

Required Requirements

• B.S. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution
• B.S. or M.S. degree, with 4+ years of training/experience in at least one of the following technologies: qPCR, Nanostring, and/or NGS, OR
• Ph.D., with 1+ year of training/experience in at least one of the following technologies: qPCR, Nanostring, and/or NGS

Preferred Requirements

• M.S. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution or Ph.D. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution
• ASCP Board Certification as a Specialist in Molecular Biology
• Excellent oral and written communication skills
• Attention to detail
• Experience in a high complexity CLIA testing environment
• Experience with data analysis and reporting of results in at least one of the following technologies: qPCR, Nanostring, and/or NGS
• Substantial experience in troubleshooting molecular laboratory techniques
• Experience preparing for/participating in laboratory audits, from CAP and other regulatory agencies

Benefits

• Medical, Vision & Dental benefits from the 1st of the month following start date
• 20 days PTO per year, accrued monthly following start date
• 12 holidays per year as well as one day for Annual Diversity Day
• Company paid Long and Short‑term disability along with Life Insurance
• 401k company contribution
• Professional development programs/ continuous learning opportunities

Almac Group, Inc. is an Equal Opportunity Employer – Minorities/Women/Protected Veterans/Disabled – Proudly embracing diversity in all of its expressions.

EEO is the Law. EEO is the Law GINA Supplement

Almac provides reasonable accommodations to people with disabilities who need assistance completing the application process. Please email us at [e-mail] to request assistance.