Clinical Genomic Technologist II

The Jackson Laboratory•Farmington, CT

About The Position

The Clinical Genomics Technologist will be responsible for processing both clinical and research samples using cutting-edge technologies for nucleic acid analysis, including but not limited to next-generation sequencing, Sanger sequencing, ddPCR and associated sample preparation technologies. These activities will be performed under CLIA/CAP regulations and will directly impact human health and thus must meet the highest possible standards for quality and integrity. The Clinical Genomics Technologist I, II, or III are distinguishable primarily by level of experience, supervision required, proficiency in problem solving, certification and wider range of training. KEY RESPONSIBILITIES: This role is responsible for the efficient and quality execution of sample accessioning, processing and data generation for the Advanced Precision Medicine Laboratory. This includes working with the Supervisor to maintain all documentation required for operation under CLIA/CAP certification, including review and writing of SOPs as necessary and use of sample tracking systems in accordance with standard operating procedures. (80% level I, 65% level II, 45% level III) Timely completion of training assigned by management or CLD to meet the needs of laboratory operations. Ensure sample accessioning is performed in an accurate manner to enable effective testing of samples downstream as ordered. Work with pathologist to evaluated neoplastic content of sample as needed. Sample processing including nucleic acid purification and preparation for sequencing and PCR is performed per established processes. Accurate and timely maintenance of operational metrics. Maintains and updates associated process documentation, participates in continuous process improvements and ongoing training. Performs quality control of samples processed and data generated prior to sending to next steps. Maintenance of auxiliary and capital equipment and instrumentation This role is also responsible for the development and validation of new methodologies, including establishing novel workflows, evaluating new instrumentation and protocols as deemed necessary by the clinical laboratory manager and/or director (20% level I, 35% level II, 55% level III). Makes technological/scientific contributions to development projects. Research, evaluate, and implement new and emerging applications and tools to improve current clinical offerings and to support new clinical offerings. This will involve working closely and coordinating with regulatory, computational sciences, IT, and management groups in accordance with established professional development goals.

Requirements

Bachelor’s and/or Master’s degree in biological or chemical sciences with experience in a regulated laboratory environment (CLIA/CAP)
Clinical Genomics Technologist II Bachelor’s with 3 years’ experience OR Master’s with 1 year’s experience
Experience in product/clinical/research assay development for clinical genomics
Well organized, with strong attention to detail and process is required.
Ability to learn new tasks and procedures in appropriate timeframes
Experience in data management, including laboratory information management systems
Excellent written and verbal skills as would be required to communicate scientific details and respond to custom inquiries.

Nice To Haves

ASCP Certification in Molecular Biology

Responsibilities

Efficient and quality execution of sample accessioning, processing and data generation for the Advanced Precision Medicine Laboratory.
Maintain all documentation required for operation under CLIA/CAP certification, including review and writing of SOPs as necessary and use of sample tracking systems in accordance with standard operating procedures.
Timely completion of training assigned by management or CLD to meet the needs of laboratory operations.
Ensure sample accessioning is performed in an accurate manner to enable effective testing of samples downstream as ordered.
Work with pathologist to evaluated neoplastic content of sample as needed.
Sample processing including nucleic acid purification and preparation for sequencing and PCR is performed per established processes.
Accurate and timely maintenance of operational metrics.
Maintains and updates associated process documentation, participates in continuous process improvements and ongoing training.
Performs quality control of samples processed and data generated prior to sending to next steps.
Maintenance of auxiliary and capital equipment and instrumentation
Development and validation of new methodologies, including establishing novel workflows, evaluating new instrumentation and protocols as deemed necessary by the clinical laboratory manager and/or director
Makes technological/scientific contributions to development projects.
Research, evaluate, and implement new and emerging applications and tools to improve current clinical offerings and to support new clinical offerings.
Working closely and coordinating with regulatory, computational sciences, IT, and management groups in accordance with established professional development goals.