Scientist II - Clinical Genomics

Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. Scientist II – Clinical Genomics Location: Iselin, NJ. Work Schedule: This is a 1st shift position primarily onsite due to the hands‑on laboratory responsibilities with occasional remote work opportunities for documentation, data analysis, or planning activities. Position Summary We are seeking an initiative‑taking and technically skilled Assay Development and Validation Scientist to join our clinical genomics laboratory. This role is heavily focused on hands‑on laboratory work, with the primary responsibility centered on the technical execution of complex R&D experiments, design and execution of validation studies, and continuous improvement of existing assays and workflows. The ideal candidate will bring deep expertise in next‑generation sequencing (NGS) and other high‑complexity genomic technologies, along with strong analytical and technical writing capabilities. Minimum Qualifications Ph.D. in Molecular Biology, Genetics, or Biochemistry or Bachelor of Science degree with 4 or more years of experience in a clinical, diagnostic, or GMP‑regulated laboratory. 1 or more years of experience with Next‑Generation Sequencing (NGS) technologies and workflows. 1 or more years of experience with genetic testing methodologies (PCR, qPCR, ddPCR, microarrays, or library preparation techniques). Preferred Qualifications 1 or more years of experience with assay validation, method comparison, and performance qualification studies in a regulated environment (CLIA, CAP, or GMP). 1 or more years of experience supporting assay transfer, scale‑up, or commercialization efforts. Additional Job Standards Ability to demonstrate exceptional technical writing skills, with experience in preparing validation plans, reports, and SOPs. Ability to effectively analyze, problem‑solve and design experiments. Ability to effectively demonstrate a high attention to detail, quality, and regulatory compliance. Ability to manage multiple projects and priorities in a fast‑paced environment. Ability to effectively communicate and collaborate across cross‑functional teams. Pay Range $90k – $129k annual (USD) 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. Employees regularly scheduled to work less than 20 hours, casual, intern, and temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. Equal Opportunity Statement Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. #J-18808-Ljbffr Labcorp