About the position
Quest Diagnostics is a leading clinical laboratory dedicated to providing innovative diagnostic information services. We are at the forefront of oncology diagnostics, leveraging advanced Next-Generation Sequencing (NGS) technologies to deliver life-changing insights. As we expand our offerings in Minimal Residual Disease (MRD) testing and early cancer detection, we are looking for a passionate Sr. Data Analyst to join our team. The Sr.Data Analyst will play a critical role in unlocking the value of complex genomic, clinical, and operational data. This role will work cross-functionally alongside Laboratory and Clinical Operations, R&D, and Bioinformatics to drive data-informed decisions that support the scaling and optimization of our MRD assays. The ideal candidate will have a strong analytical mindset, a deep understanding of laboratory data workflows, and a passion for improving patient outcomes through precision oncology.
Responsibilities
• Analyze complex datasets related to MRD assay performance, laboratory turnaround times, and clinical validity.
• Design, build, and maintain automated dashboards to communicate key metrics to cross-functional stakeholders.
• Partner with the R&D and Product Development teams to provide analytical support for the design, validation, and commercialization of new early-detection oncology and MRD assays.
• Work closely with Bioinformatics engineers to analyze pipeline outputs and support the strategic scaling of robust data pipelines.
• Ensure all data management and reporting processes align with strict regulatory standards (e.g., FDA, ISO, IEC).
• Support documentation and risk management efforts as part of a robust Software Development Life Cycle (SDLC) for our NGS systems.
• Identify bottlenecks in laboratory workflows and propose data-backed solutions to improve testing efficiency, accuracy, and scalability.
Requirements
• 3+ years of experience in data analysis, preferably within a clinical laboratory, biotech, academia or healthcare setting.
• Familiarity with genomic data, bioinformatics workflows, and clinical assay validation.
• Understanding of regulatory compliance frameworks (FDA, CLIA, CAP, ISO) and software quality standards.
• High proficiency in querying and manipulating large datasets using SQL.
• Strong programming skills in Python or R for statistical analysis and data modeling.
• Experience with data visualization tools (e.g., Tableau, Power BI, Metabase).
• Exceptional problem-solving skills and the ability to translate complex technical findings into clear, strategic business recommendations.
• Strong communication and collaboration skills with a proven track record of working effectively across scientific, technical, and business teams.
Nice-to-haves
• Exposure to oncology diagnostics, NGS data, and/or MRD testing is highly preferred.
Benefits
• Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
• Best-in-class well-being programs
• Annual, no-cost health assessment program Blueprint for Wellness®
• healthyMINDS mental health program
• Vacation and Health/Flex Time
• 6 Holidays plus 1 "MyDay" off
• FinFit financial coaching and services
• 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
• Employee stock purchase plan
• Life and disability insurance, plus buy-up option
• Flexible Spending Accounts
• Annual incentive plans
• Matching gifts program
• Education assistance through MyQuest for Education
• Career advancement opportunities