Sr. Data Analyst, MRD & Oncology Diagnostics

Pay Range: $80,000.00 - $100,000.00 / year Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation.   Benefits Information: We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives.

Our pay and benefit plans have been designed to promote employee health in all respects – physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include: · 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 · and so much more!

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.

Data-Driven Insights & Reporting: 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. Cross-Functional Collaboration: 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.

Bioinformatics & Pipeline Support: Work closely with Bioinformatics engineers to analyze pipeline outputs and support the strategic scaling of robust data pipelines. Regulatory Compliance & Quality: 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.

Operational Excellence: Identify bottlenecks in laboratory workflows and propose data-backed solutions to improve testing efficiency, accuracy, and scalability. Required Work Experience: 3+ years of experience in data analysis, preferably within a clinical laboratory, biotech, academia or healthcare setting. Preferred Work Experience: Exposure to oncology diagnostics, NGS data, and/or MRD testing is highly preferred.

Knowledge: 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.