Clinical Molecular Technologist

PURPOSE:
Must be authorized to work in the United States. With minimal oversight from the Manager/Supervisor of the Laboratory, the Molecular 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, qPCR and associated sample preparation technologies. These activities are performed under CLIA/CAP regulations and will directly impact human health and thus must meet the highest possible standards for quality and integrity. Technologist roles are distinguishable primarily by level of experience, supervision required, proficiency in problem solving, certification and wider range of training.
Different schedules available.
Must have experience performing NGS assays in a high complexity clinical laboratory.
KEY RESPONSIBILITIES:
This role is responsible for the efficient and quality execution of sample accessioning, processing and data generation for the Laboratory. This includes working with the manager 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.
Timely completion of training assigned by management or laboratory director 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
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
MINIMUM QUALIFICATIONS:
Education and Experience Requirements – Bachelor’s and/or Master’s degree in biological or chemical sciences with experience in a regulated laboratory environment (CLIA/CAP), and ASCP Certification in Molecular Biology
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

Employment type
Full-Time

Work arrangement
No