Clinical Laboratory Technologist
Schedule:
"Mon–Tues & Fri–Sat 12:30pm–11:00pm"
OR
"Sat–Sun 8:00am–6:30pm & Mon–Tues 12:30pm–11:00pm"
Comp : $30 - $44/hr
About the role
Join a high-volume clinical genomics team processing patient and research specimens through next-generation sequencing workflows. You'll run DNA extraction, PCR amplification, and library prep on liquid-handling automation platforms, with results flowing directly to oncologists, clinicians, and research partners. Our laboratories operate under CLIA, CAP, NYS, and FDA frameworks — regulatory precision is built into everything we do.
Day-to-day responsibilities
- Execute DNA extraction, PCR, and high-throughput sequencing protocols within a compliant QMS
- Operate liquid-handling robotics and next-generation sequencers;
perform routine maintenance and troubleshooting - Complete assigned runs — clinical specimens, reagent QC batches, validation studies, and special projects — accurately and on schedule
- Log non-conformances, enter run data into the LIMS, and maintain documentation to Good Documentation Practice standards
- Uphold GxP, GMP, GCP, and GLP requirements;
fulfill high-complexitytesting personnel obligations under 42 CFR - Maintain continuing education credits required by applicable regulatory bodies
- Handle human biological specimens and biohazardous materials according to established safety protocols
Seniority levels
We hire at three levels based on experience and demonstrated competency:
(Level I)
- Performs protocols with some supervisory guidance;
escalates issues to lead or supervisor - Resolves routine and occasional novel process variations using up-to-date information
- Communicates clearly during shift handoffs;
keeps detailed records - May provide informal guidance to newer colleagues
(Level II)
- Works with minimal direction;
exercises considerable clinical initiative - Conducts training and competency evaluations for technician-level staff on high-complexity methods
- Proposes procedural improvements to enhance team efficiency;
understands when to escalate quality or timeline concerns
(Level III)
- Operates independently;
regularly applies educated discretion in decision-making - Drives process change recommendations backed by cross-functional knowledge
- Proficient in laboratory automation and recognized for best-practice leadership
Qualifications
(Level I) — must meet one of the following
- Bachelor's degree or higher in medical technology or laboratory science, or
- Bachelor's degree or higher in a chemical or biological science plus at least 6 months of high-complexity molecular experience in a CLIA-certified laboratory
(Level II) — must meet all of the following
- Bachelor's degree or higher in a relevant science or laboratory science field
- Minimum 1 year of clinical lab experience in a high-complexity CLIA setting (or 2 years with a Master's degree or higher)
- Minimum 3 years of hands-on molecular laboratory experience (or 2 years with a Master's or higher)
(Level III) — must meet all of the following
- Bachelor's degree or higher in a relevant science or laboratory science field
- Minimum 3 years of clinical lab experience in a high-complexity CLIA setting (or 2 years with a Master's degree or higher)
- Minimum 5 years of molecular laboratory experience (or 3 years with a Master's or higher)
- Demonstrated proficiency in laboratory automation and best practices