The University of Texas MD Anderson Cancer Center
Clinical Laboratory Scientist
The University of Texas MD Anderson Cancer Center, San Diego, California, United States, 92189
Job Title: Clinical Laboratory Scientist
Job Number:
36688 Location:
San Diego,CA Job Description The Clinical Laboratory Scientist (CLS) is responsible for performing complex clinical laboratory testing with a primary focus on nucleic acid isolation/extraction and Next-Generation Sequencing (NGS) workflows and analysis. This role requires adherence to established procedures, compliance with quality and regulatory standards, and effective communication with laboratory leadership. Under minimal supervision, the CLS will contribute to the setup, execution, and reporting of high-throughput molecular oncology assays and provide supervisory oversight within a CLIA-licensed and CAP-accredited laboratory. Responsibilities Perform nucleic acid isolation, library preparation, NGS techniques, and other molecular biology methods with strict adherence to aseptic technique.
Function as a
General Supervisor
in a CLIA-licensed and CAP-accredited clinical laboratory, including: Supervising day-to-day performance of high-complexity testing.
Providing on-site supervision during high-complexity testing.
Monitoring test analyses and specimen examinations to ensure compliance with quality standards.
Conduct specimen processing (e.g., accessioning, aliquoting, dilutions, sample problem resolution).
Perform clinical testing of patient samples, data analysis, and interpretation of results for review and approval by the Laboratory Director.
Prepare and manage reagents, maintain instruments, and perform validation and preventative maintenance activities.
Maintain accurate documentation, records, and compliance with SOPs, laboratory policies, and safety procedures.
Support quality systems by: Managing document control for SOPs, policies, and related materials.
Assisting in root cause analysis, Corrective and Preventative Actions (CAPA), and quality/process improvement initiatives.
Supporting regulatory audits, inspections, and continuous laboratory readiness.
Contribute to technology transfer of new processes and methods from R&D to clinical operations.
Assist in training laboratory staff and coordinating internal proficiency testing.
Adhere to all applicable regulatory guidelines, including CLIA/CMS, CAP, NYSDOH, and ISO 13485.
Obtain and maintain Continuing Education credits to ensure an active, valid California CLS license.
Required Skills Bachelors degree (or higher) in Biology, Genetics, Molecular Biology, or a related field.
Valid, current California CLS license (generalist or limited CGBMS).
Minimum 24 years of experience in a CLIA-licensed, CAP-accredited clinical laboratory.
Hands-on experience with molecular biology techniques, including nucleic acid extraction, PCR, and NGS workflows.
Proficiency in Quality Management Systems within a regulated clinical laboratory environment.
Strong knowledge of federal, state, and accrediting agency requirements (CLIA, CAP, FDA, etc.).
Excellent analytical, problem-solving, and data interpretation skills.
Demonstrated ability to work both independently and collaboratively in a fast-paced environment.
Strong organizational, multitasking, and communication skills with attention to detail.
Additional Responsibilities
May serve as Quality Assurance Coordinator, Quality Systems Manager, or Management Representative.
May carry out delegated responsibilities from the Laboratory Director as documented.
Perform other duties as assigned to support laboratory operations.
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36688 Location:
San Diego,CA Job Description The Clinical Laboratory Scientist (CLS) is responsible for performing complex clinical laboratory testing with a primary focus on nucleic acid isolation/extraction and Next-Generation Sequencing (NGS) workflows and analysis. This role requires adherence to established procedures, compliance with quality and regulatory standards, and effective communication with laboratory leadership. Under minimal supervision, the CLS will contribute to the setup, execution, and reporting of high-throughput molecular oncology assays and provide supervisory oversight within a CLIA-licensed and CAP-accredited laboratory. Responsibilities Perform nucleic acid isolation, library preparation, NGS techniques, and other molecular biology methods with strict adherence to aseptic technique.
Function as a
General Supervisor
in a CLIA-licensed and CAP-accredited clinical laboratory, including: Supervising day-to-day performance of high-complexity testing.
Providing on-site supervision during high-complexity testing.
Monitoring test analyses and specimen examinations to ensure compliance with quality standards.
Conduct specimen processing (e.g., accessioning, aliquoting, dilutions, sample problem resolution).
Perform clinical testing of patient samples, data analysis, and interpretation of results for review and approval by the Laboratory Director.
Prepare and manage reagents, maintain instruments, and perform validation and preventative maintenance activities.
Maintain accurate documentation, records, and compliance with SOPs, laboratory policies, and safety procedures.
Support quality systems by: Managing document control for SOPs, policies, and related materials.
Assisting in root cause analysis, Corrective and Preventative Actions (CAPA), and quality/process improvement initiatives.
Supporting regulatory audits, inspections, and continuous laboratory readiness.
Contribute to technology transfer of new processes and methods from R&D to clinical operations.
Assist in training laboratory staff and coordinating internal proficiency testing.
Adhere to all applicable regulatory guidelines, including CLIA/CMS, CAP, NYSDOH, and ISO 13485.
Obtain and maintain Continuing Education credits to ensure an active, valid California CLS license.
Required Skills Bachelors degree (or higher) in Biology, Genetics, Molecular Biology, or a related field.
Valid, current California CLS license (generalist or limited CGBMS).
Minimum 24 years of experience in a CLIA-licensed, CAP-accredited clinical laboratory.
Hands-on experience with molecular biology techniques, including nucleic acid extraction, PCR, and NGS workflows.
Proficiency in Quality Management Systems within a regulated clinical laboratory environment.
Strong knowledge of federal, state, and accrediting agency requirements (CLIA, CAP, FDA, etc.).
Excellent analytical, problem-solving, and data interpretation skills.
Demonstrated ability to work both independently and collaboratively in a fast-paced environment.
Strong organizational, multitasking, and communication skills with attention to detail.
Additional Responsibilities
May serve as Quality Assurance Coordinator, Quality Systems Manager, or Management Representative.
May carry out delegated responsibilities from the Laboratory Director as documented.
Perform other duties as assigned to support laboratory operations.
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