Clinical Laboratory Technologist

Clinical Laboratory Technologist

Schedule: M–F, 2:30 pm–11 pm (fully onsite)

Comp: $30 - $55/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-complexity testing personnel obligations under 42 CFR 493.1495
• 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