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Clinical Research Jobs in New Jersey, USA | Global Life Science Career Opportunities at Labcorp

Clinical Research Jobs in New Jersey, USA | Jobs at Labcorp 

Step into a rewarding career at the forefront of laboratory excellence. This Clinical Laboratory QA Coordinator opportunity empowers life science professionals to impact patient care, regulatory compliance, and operational quality in a rapidly growing global healthcare environment. Designed for detail-driven experts, these Clinical Research Jobs offer stability, purpose, and advancement within one of the world’s most respected life science organizations.

About the Company

Labcorp is a global life sciences leader committed to improving health and delivering world-class diagnostic solutions. With a presence in more than 100 countries, Labcorp empowers clinicians, researchers, and patients through high-quality laboratory operations, advanced technologies, and a mission-driven approach to healthcare innovation.

Job Details

  • Job Title: Clinical Laboratory QA Coordinator – Molecular & Microbiology
  • Location: Raritan, NJ
  • Category: Regulatory/Compliance
  • Job ID: 2535880
  • Type: Full-Time | On-site
  • Pay Range: $29.00–$33.00/hr
  • Schedule: Monday–Friday, 8:30 AM–5:00 PM

About the Role

Labcorp is seeking a Laboratory Quality Assurance Coordinator to support quality systems across molecular and microbiology laboratories. This role is ideal for laboratory professionals with strong attention to detail and a passion for quality and compliance.

Job Responsibilities

  • Support quality assurance, quality control, improvement, and training activities.
  • Prepare laboratories for regulatory inspections and provide onsite inspection support.
  • Maintain documentation required for accreditation and regulatory audits.
  • Track and coordinate internal and external proficiency testing.
  • Perform internal audits and prepare corresponding reports.
  • Generate recurring quality reports for laboratory operations.
  • Stay current on regulatory requirements (CAP, CLIA, ISO) and proficiency testing guidelines.
  • Initiate and maintain Master Control forms for audits.
  • Participate in monthly quality meetings and prepare meeting minutes.
  • Perform administrative and clerical tasks as needed.

Requirements for Clinical Research Jobs

  • Bachelor’s degree in Biological Sciences, Clinical Laboratory Science, or equivalent per CLIA/State requirements.
  • Minimum 1 year of experience as a technologist or in a quality-related role.
  • Clinical laboratory experience strongly preferred.
  • Experience in microbiology and/or molecular testing preferred.
  • Knowledge of CAP/CLIA/ISO regulations and licensing requirements.
  • Understanding of audit requirements and quality assurance practices.
  • Strong analytical, critical-thinking, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • High attention to detail with strong organizational abilities.
  • Ability to work independently and as part of a team.
  • Proficiency in MS Office and strong general computer skills.

Benefits for Clinical Research Jobs

  • Employees working 20+ hours/week are eligible for:
    • Medical, Dental, Vision
    • Life Insurance, STD/LTD
    • 401(k), PTO/FTO
    • Tuition Reimbursement
    • Employee Stock Purchase Plan
  • Part-time employees under 20 hrs/week are eligible for 401(k) only.

APPLY ONLINE HERE

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