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.

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📌 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)
• Application Deadline: March 27, 2026

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🎯 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

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🎓 Qualifications Required

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

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💻 Required Skills

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

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💰 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

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🚀 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

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📥 How to Apply

Application Link