If you’re looking to build a career in clinical research sample management, this opportunity from Labcorp could be a strong fit. The company is hiring for the role of Sample Information Coordinator II in Bengaluru, offering exposure to LIMS systems, study coordination, and clinical sample workflows.

This role is ideal for candidates with an MSc in Biochemistry, Biotechnology, or Microbiology who want to work in a structured, regulated clinical research environment.

🔍 Job Overview

• Role: Sample Information Coordinator II
• Company: Labcorp
• Location: Bengaluru, India
• Job Type: Full-time (Office-based)
• Shift: 2nd Shift (India)
• Application Deadline: May 1, 2026

📌 Key Responsibilities

As a Sample Information Coordinator, you will play a critical role in ensuring accurate sample tracking and data integrity within clinical studies:

• Support Study Director (SD), Principal Investigator (PI), and Study Coordinator (SC) in study sample setup
• Prepare and verify demographic import files and tube labeling
• Ensure accurate protocol interpretation for sample handling
• Maintain and update LIMS (Laboratory Information Management System)
• Identify and resolve sample discrepancies and data inconsistencies
• Coordinate with sample management teams to ensure timely issue resolution
• Monitor sample logging schedules for readiness before analysis
• Review QAU audit reports and submit responses
• Ensure timely sample receipt communication to sponsors/sites
• Perform sample reconciliation and documentation management
• Participate in client interactions and site visits

🎓 Qualifications Required

• Educational Qualification:
  • MSc in Biochemistry / Biotechnology / Microbiology
• Skills & Experience:
  • Experience in sample management or LIMS systems
  • Knowledge of Watson application (preferred)
  • Strong data validation and documentation skills
  • Proficiency in MS Word, Excel, and database tools
  • Attention to detail and problem-solving ability

💼 Benefits of Working at Labcorp

• Opportunity to work in a global clinical research organization
• Hands-on experience with LIMS and regulated environments
• Exposure to clinical trials and sponsor interactions
• Inclusive workplace with strong diversity and compliance policies
• Career growth in clinical data and sample coordination roles

📝 How to Apply

Application Link