Sr. Research Associate - R&D Next Generation Sequencing
LabcorpAbout the role
Do you have a passion for science? Do you enjoy working in a collaborative environment? If so, take your career to the next level as a Senior Research Associate and contribute to the advancement of cutting-edge molecular diagnostics on our dynamic R&D Next Generation Sequencing team in Westborough, MA. Be a part of this life-saving work and help improve patients' lives while growing your career.
Position Summary
Labcorp is a leading diagnostic reference laboratory dedicated to delivering high-quality, clinically actionable results through innovative molecular technologies. The R&D team plays a critical role in developing and validating molecular assays that directly impact patient care.
As a Senior Research Associate, you will support all R&D functions that pertain to the launch of a molecular test into a clinical laboratory from development and validation to implementation and troubleshooting. This bench-focused position requires a strong foundation in molecular biology and deep familiarity with NGS technologies. This position will also involve working collaboratively with other groups throughout Labcorp in a variety of areas as they apply to translational research in a clinical diagnostics context.
Candidates given the best consideration will have the following:
Minimum 5 years of hands-on molecular biology experience, with at least 3 years in a clinical diagnostics, biotech or research lab setting
Firm understanding of fundamental molecular biology and genetics concepts
Expertise in NGS technologies and workflows, including library prep and target enrichment
Hands-on experience with standard molecular biology techniques, including nucleic acid extraction and quantification, PCR, qPCR and Sanger sequencing
Strong organizational, documentation and analytical thinking skills
Proficient with webtools and databases for assay design, data analysis, literature searches
Familiarity with Microsoft Office apps; proficiency in statistical analysis a plus
Ability to work with minimal to moderate supervision in a dynamic environment and under tight deadlines
Preferred Qualifications:
Understanding of clinical molecular assay validation requirements
Experience with automation platforms and high-throughput molecular workflows
Knowledge of bioinformatics tools used for NGS data review and quality control
Education
Minimum of a bachelor’s degree in biology, Genetics, Biochemistry, or related field
Master’s degree preferred
Key Responsibilities
Provide hands-on support in the design, optimization and execution of complex molecular workflows with particular emphasis on NGS assay development
Contribute to the analytical validation of NGS assays, including reproducibility, sensitivity, specificity, and limit of detection studies.
Assist in preparing documentation for regulatory submissions, validation plans and standard operating procedures (SOPs)
Support technology transfers from R&D to clinical operations through training and cross-functional collaboration
Analyze experimental data and troubleshoot technical issues in collaboration with the bioinformatics and clinical laboratory staff
Summarize and present results within and outside of the R&D group
Evaluate commercial products for applicability in a clinical lab setting
Generate manuscripts for submission to peer-reviewed journals
Keep abreast of current literature pertinent to the project or departmental areas of interest
Support routine lab activities, e.g. maintaining equipment, ordering/receiving supplies
Perform other duties as assigned and contribute to a collaborative, high-quality lab culture
Pay Range: $75k - $85k (USD)
All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please
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