Labcorp Hiring Sample Information Coordinator | Freshers

If you are looking to build a career in clinical research operations, sample management, or LIMS systems, this opportunity from Labcorp India is highly relevant. Labcorp is hiring for the position of Sample Information Coordinator I in Bengaluru, offering exposure to global clinical studies and laboratory workflows.

This role is ideal for candidates with MSc in Biotechnology, Microbiology, or Biochemistry, especially those interested in non-lab, data-driven clinical roles.


📌 Job Overview

  • Role: Sample Information Coordinator I
  • Company: Labcorp
  • Location: Bengaluru, Karnataka, India
  • Job Type: Full-Time
  • Shift: 2nd Shift (India)
  • Experience: Freshers / Entry-Level
  • Qualification: MSc (Biochemistry / Biotechnology / Microbiology)

🎯 Key Responsibilities

1. Study Sample Coordination

  • Assist Study Director (SD), Principal Investigator (PI), and Study Coordinator (SC) in study setup
  • Support preparation of sample demographic import files
  • Coordinate tube label generation and verification

2. LIMS & Data Management

  • Maintain and update LIMS (Laboratory Information Management System)
  • Ensure consistency between:
    • Tube labels
    • LIMS data
    • Study documentation

3. Data Quality & Discrepancy Handling

  • Identify and resolve data discrepancies in sample records
  • Perform demographic checks for study samples
  • Ensure accurate protocol interpretation

4. Sample Lifecycle Management

  • Monitor sample logging schedules
  • Support sample reconciliation processes
  • Maintain organized and audit-ready study files

5. Communication & Coordination

  • Interact with internal teams and clients when required
  • Assist in resolving sample-related queries

🎓 Qualifications Required

  • MSc in:
    • Biochemistry
    • Biotechnology
    • Microbiology
  • Basic understanding of:
    • Clinical research workflows
    • Sample management systems
  • Familiarity with:
    • LIMS (preferred)
    • Watson Application (added advantage)

💻 Required Skills

  • Strong attention to detail
  • Good documentation practices (GDP)
  • Proficiency in:
  • Ability to manage structured data and workflows

💰 Salary & Benefits (Estimated)

  • Salary Range: ₹3.0 – ₹4.5 LPA (industry standard for entry-level roles)
  • Exposure to global clinical trials and laboratory systems
  • Opportunity to transition into:
    • Clinical Data Management (CDM)
    • Pharmacovigilance (PV support roles)
    • Clinical Operations

🚀 Why This Role is Important

This is a highly strategic entry point for candidates who:

  • Want to move away from QC lab work
  • Prefer computer-based clinical roles
  • Aim for careers in:
    • Clinical Data Management
    • Regulatory Operations
    • Trial Master File (TMF)
    • Clinical Project Support

📥 How to Apply

Application Link

By Admin

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