Senior Research Associate- Diagnostic Assay Development

• Hands-on execution of complex single-cell and spatial genomics assays (e.g., sample processing, library preparation, sequencing).
• Systematically troubleshoot, optimize, and refine specific steps within the assay workflow to improve performance, robustness, and efficiency.
• Perform feasibility studies on new reagents, instrumentation, and process improvements for clinical readiness.
• Prepare and process samples in support of large-scale clinical research studies

• Generate and maintain meticulous laboratory records, protocols (SOPs), and batch records following Good Documentation Practices (GDP).
• Execute formal experiments for analytical validation studies, including assessment of accuracy, precision, limit of detection, and reproducibility.
• Ensure all work is conducted under appropriate quality controls
• Present experimental data clearly and concisely in team meetings and written reports.

• Support the transfer of robust assay workflows to the CLIA operations team.
• Collaborate closely with R&D Scientists, Automation Engineers, and Bioinformatics teams to meet project milestones.
• Work closely with the internal lab operations team to support the maintenance of a high-quality, organized laboratory environment, including inventory management and forecasting, equipment calibration, and ensuring compliance with safety standards.

• B.S. or M.S. in Molecular Biology, Genetics, Biochemistry, or a related scientific field.
• B.S. with 5+ years or M.S. with 3+ years of hands-on experience in molecular diagnostics or genomics assay development in an industry setting.
• Direct, demonstrable experience with advanced molecular technologies, particularly Next-Generation Sequencing (NGS) workflows
• Exceptional proficiency in molecular biology techniques, including nucleic acid extraction, PCR/qPCR, and NGS library preparation
• A proven track-record of using and optimizing and troubleshooting molecular biology protocols.
• Experience working with challenging clinical sample types (e.g., FFPE tissue, primary tumor cells, low-input samples).
• Experience working within a quality system or environment governed by CLIA, CAP, or ISO 13485 standards strongly preferred.
• Prior hands-on experience with 10x Genomics single-cell or spatial technologies (e.g., Chromium or Xenium platforms) is a strong advantage.
• Experience with automated liquid handling for high-throughput assay execution is a strong advantage; experience with microscopy techniques a plus

• Ability to organize, analyze, and interpret complex data sets (e.g., assay metrics, quality control data) and effectively troubleshoot issues based on results.
• Commitment to rigorous execution, meticulous record-keeping, and high standards of scientific quality.
• Possess excellent communication skills, and can effectively collaborate with interdisciplinary teams, integrating their feedback into your experimental design.
• Thrive in fast-paced environments, and excel at managing multiple priorities, adapting to change, and consistently delivering results.

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