Clinical Laboratory Associate, PM Shift (Contract)
About The Position
Join ClearNote Health and apply your clinical laboratory skills to help beat cancer. Our proprietary epigenomics technology detects cancer early, leading to better outcomes for patients. Our tests are developed by generating and analyzing genome-wide sequence profiles. Talented and dedicated clinical laboratory team members are vital to help deliver quality lifesaving results from our testing platform. We are seeking a clinical laboratory associate committed to supporting the growth and operation of our CLIA certified and CAP accredited laboratory. You will assist with the day-to-day testing operations including accessioning and labeling of patient specimens and assisting with instrument maintenance and specimen processing. This role requires a Monday – Friday 3:00 pm – 11:30 pm schedule
Requirements
- AS degree or equivalent in biological sciences or related degree.
- Excellent interpersonal, team, written, and spoken communication skills .
- Ability to operate various laboratory information management systems (LIMS).
- Must be able to work Monday to Friday 3:00 pm -11:30 pm
Nice To Haves
- Bachelor’s degree in biological sciences a plus.
Responsibilities
- Accession patient samples and ensure specimen acceptance criteria are met.
- Prepare labels and consumables for downstream processing.
- Engage in continuous process and service improvement.
- Ensure QC and maintenance of all laboratory equipment.
- Support good laboratory practices (GLP) and decontaminate work environments regularly.
- Adhere to good documentation practices (GDP) when notating on document-controlled forms.
- Maintain working knowledge of laboratory policies and procedures.
- Document reagent and consumable information when received at the laboratory.
- Documenting procurement issues, updates, and data entry into LIMS systems.
- Receive and store shipments arriving onsite.
- Storage of patient specimens and retrieval of samples needed for repeat testing.
- Assess discrepancies with test requisition forms and patient specimens.
- Assist licensed personnel in all modules of clinical NGS workflows, automation troubleshooting, and reagent preparation.
- Help coordinate reagent qualifications and documentation for verification of new lots.
- Evaluate new process improvements and make appropriate recommendations based on thorough evaluation of technical, quality, and efficiency impact.
- Ensure all work is in accordance with state and federal regulations, organizational policy, and accreditation/compliance requirements.
- Review and contribute to the writing of standard operating procedures (SOPs).
Benefits
- We provide generous benefits to all employees including stock options.
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What This Job Offers
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
1-10 employees
