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Scientist Ii - Clinical Genomics

Labcorp
1-4+ years
USD $90,000 – $129,000 per year (approximately ₹77 lakh – ₹1.1 crore annually)
Remote, India, India
10 June 11, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Scientist II – Clinical Genomics

Company: Labcorp
Location: Iselin
Job Type: Full-Time
Work Model: Primarily Onsite (1st Shift) with occasional remote work for documentation, data analysis, and planning activities.

Experience Level

  • PhD in Molecular Biology, Genetics, Biochemistry, or related field
    OR

  • Bachelor's degree with 4+ years of experience in a clinical, diagnostic, or GMP-regulated laboratory

  • 1+ year experience in NGS technologies and workflows

  • 1+ year experience in genetic testing methodologies (PCR, qPCR, ddPCR, microarrays, library preparation)

Salary

USD $90,000 – $129,000 per year (approximately ₹77 lakh – ₹1.1 crore annually).

Role Summary

Labcorp is seeking a Scientist II – Clinical Genomics to support assay development, validation, and optimization activities within a clinical genomics laboratory. The position involves significant hands-on laboratory work focused on next-generation sequencing (NGS), validation studies, and continuous improvement of genomic testing workflows.

Key Responsibilities

Assay Development & Validation

  • Design and execute complex R&D experiments.

  • Develop and optimize genomic assays.

  • Conduct assay validation and performance qualification studies.

  • Perform method comparison and verification studies.

Genomic Testing & Laboratory Operations

  • Work with NGS platforms and workflows.

  • Perform molecular biology techniques including PCR, qPCR, ddPCR, and library preparation.

  • Support implementation of new testing methodologies.

Data Analysis & Scientific Documentation

  • Analyze experimental and validation data.

  • Prepare validation protocols and reports.

  • Develop and maintain SOPs and technical documentation.

  • Ensure compliance with regulatory and quality requirements.

Cross-Functional Collaboration

  • Work closely with laboratory, quality, regulatory, and operational teams.

  • Support assay transfer, scale-up, and commercialization activities.

  • Participate in troubleshooting and process improvement initiatives.

Required Qualifications

  • PhD in Molecular Biology, Genetics, Biochemistry, or related discipline
    OR

  • Bachelor's degree with 4+ years relevant laboratory experience.

  • Experience with NGS technologies.

  • Experience with molecular diagnostic techniques.

  • Strong experimental design and problem-solving abilities.

Preferred Qualifications

  • Experience in CLIA, CAP, GMP, or other regulated laboratory environments.

  • Assay validation and method comparison experience.

  • Experience supporting assay transfer and commercialization projects.

Key Skills

  • Next-Generation Sequencing (NGS)

  • Molecular Diagnostics

  • PCR / qPCR / ddPCR

  • Genomics Assay Development

  • Validation Studies

  • Technical Writing

  • Data Analysis

  • Quality & Regulatory Compliance

  • Project Management

  • Scientific Problem Solving

Benefits

  • Medical, Dental, and Vision Insurance

  • Life Insurance

  • Short-Term and Long-Term Disability Coverage

  • 401(k) Retirement Plan

  • Paid Time Off (PTO)

  • Tuition Reimbursement

  • Employee Stock Purchase Plan

  • Career Development Opportunities