Clinical Laboratory Supervisor

Almac Group; Durham (NC); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical benefits

Vision benefits

Dental benefits

PTO 20 days

Holidays and Diversity Day

Disability & Life Insurance

401k

Professional development

Job summary

Almac Group in Durham, NC is seeking a Clinical Laboratory Supervisor to oversee day-to-day testing in the CLIA-accredited Clinical Testing Laboratory, including supervision of high-complexity molecular testing within global clinical trials.

You will lead scientific staff, ensure regulatory compliance, drive continuous improvement, and maintain rigorous quality and patient-care standards, while mentoring a talented team and advancing precision medicine.

Qualifications

• BS/BA degree in a relevant field from an accredited institution.
• Advanced degree with hands-on experience in qPCR, Nanostring, or NGS.
• PhD with experience in molecular testing technologies.

Responsibilities

• Provide day-to-day supervision of testing personnel and reporting of test results within the high complexity Clinical Testing Laboratory.
• Coordinate activities of junior team members to ensure timely completion of clinical testing.
• Monitor specimen examinations and analyses to maintain analytic performance at all times.
• Generate, revise, and review laboratory or equipment-related SOPs and quality documents.
• Perform molecular biological techniques adhering to QC policies.
• Ensure remedial actions are taken when test systems deviate from performance specs and leadership is notified.
• Be available for on-site, telephone, or electronic consultation to resolve technical problems.
• Monitor stock levels and coordinate ordering/testing of new reagents and controls.

Skills

Leadership

Communication

Attention to detail

Education

BS in chemical/biological/medical/clinical lab science/medical technology

BS or MS with 4+ years in qPCR/Nanostring/NGS

PhD with 1+ year in qPCR/Nanostring/NGS

Tools

qPCR

Nanostring

NGS

Job description

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 include but are not limited to:

• 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 MS 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

What can Almac Group offer you?

• 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 is an exceptional, award winning, drug development solutions provider at the forefront of the pharmaceutical industry. We are a privately owned organization that has organically grown over 50 years now employing over 7,500 highly skilled personnel worldwide. Our US Headquarters is located at Souderton, PA with additional operations scattered around the US and Europe. ‘Partnering to Advance Human Health’ is more than just a tagline – it is our way of life.

Embracing diversity is at the heart of enhancing Almac Group’s unique culture and reflects our fundamental belief that all people deserve equality, inclusivity and the opportunity for advancement. We are committed to cultivating a welcoming, supportive, and inclusive environment for all. Together, we will build on the strength in our diversity and deliver exceptional solutions to advance human health globally.

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.