SeqMatic is a CLIA-licensed, CAP-accredited contract research organization (CRO) specializing in next-generation sequencing (NGS), multiomics, and histopathology services. Founded by former Illumina R&D scientists, we support clinical and translational research through high-quality laboratory services and personalized support.
Position Summary:
We are seeking a Clinical Laboratory Scientist with a valid California CLS license to join our clinical operations team. This role involves supporting clinical trial workflows, ensuring regulatory compliance, and performing high-complexity testing in a CLIA-certified environment. The ideal candidate will have a strong background in molecular diagnostics and a passion for advancing clinical research.
Key Responsibilities:
- Conduct high-complexity molecular testing, including NGS-based assays, in compliance with CLIA/CAP regulations.
- Perform sample QC and library QC.
- Prepare sequencing libraries using established protocols.
- Operate and maintain Illumina sequencers.
- Review and validate clinical data and laboratory results for accuracy and completeness.
- Collaborate with clinical trial sponsors and internal teams to ensure protocol adherence.
- Maintain detailed documentation and contribute to regulatory submissions.
- Assist in the development and validation of new clinical assays.
- Participate in quality assurance and continuous improvement initiatives.
- Responsible for maintaining updated understanding and knowledge of methods performed in the lab
- Follows GLP (good laboratory practice): maintain clean and organized work space
- Participates in the updating of departmental standard operating procedures to accurately reflect the current practices.
- Performs quality control procedures to ensure accuracy of clinical data (if applicable)
- Assists teammates in completing daily tasks
Qualifications:
- Valid California Clinical Laboratory Scientist (CLS) license.
- Bachelor’s or Master’s degree in Clinical Laboratory Science, Molecular Biology, or related field.
- 2+ years of experience in a clinical laboratory or clinical research setting.
- Familiarity with NGS workflows and clinical assay validation preferred.
- Strong understanding of CLIA/CAP regulations and GCP guidelines.
- Excellent communication and organizational skills.
- Must be legally authorized to work in the USA.
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