Job Opportunity: Sample Information Coordinator I at Labcorp

Job Summary

Labcorp is seeking a detail-oriented and motivated professional for the position of Sample Information Coordinator I based in Bengaluru. This is an excellent entry-level opportunity for candidates holding an MSc in life sciences who are eager to build a career in clinical research operations, sample management, and data-driven laboratory workflows. As a vital part of our global clinical studies team, you will manage essential data, ensure the integrity of laboratory information systems, and support critical study operations in a professional, non-laboratory setting.

Responsibilities

As a Sample Information Coordinator I, you will play a key role in the lifecycle of clinical study samples. Your primary responsibilities will include:

• Study Sample Coordination: Collaborate with Study Directors, Principal Investigators, and Study Coordinators during study setup. You will assist in the preparation of sample demographic import files and coordinate the generation and verification of tube labels to ensure study readiness.
• LIMS and Data Management: Manage and update the Laboratory Information Management System (LIMS). You are responsible for ensuring perfect consistency between physical tube labels, digital LIMS entries, and all supporting study documentation.
• Data Quality and Discrepancy Handling: Proactively identify and resolve discrepancies in sample records. You will conduct demographic checks and ensure that all sample documentation is strictly aligned with protocol requirements.
• Lifecycle Management: Monitor sample logging schedules, facilitate sample reconciliation processes, and maintain organized, audit-ready study files at all times.
• Communication: Serve as a point of contact for internal teams and clients to resolve sample-related inquiries and maintain effective operational flow.

Requirements

We are looking for candidates who possess a strong academic foundation and a keen interest in clinical research data management.

• Education: MSc in Biotechnology, Microbiology, or Biochemistry.
• Experience: This is an entry-level/fresher-friendly role; however, a foundational understanding of clinical research workflows and sample management systems is required.
• Technical Skills: Familiarity with LIMS is highly preferred. Experience with the Watson Application will be considered an added advantage.
• Core Competencies:
  • Exceptional attention to detail and accuracy.
  • Strong understanding of Good Documentation Practices (GDP).
  • Ability to manage complex, structured data and multi-task effectively in a fast-paced environment.
  • Professional communication skills for internal and cross-functional collaboration.

Benefits

Joining Labcorp offers more than just a job; it provides a strategic entry point into the global pharmaceutical and clinical research industry.

• Career Growth: This role serves as a stepping stone for career paths in Clinical Data Management (CDM), Pharmacovigilance, Clinical Operations, Regulatory Operations, and Trial Master File (TMF) management.
• Professional Exposure: Gain firsthand experience with global clinical trial standards and industry-leading laboratory information systems.
• Compensation: We offer a competitive salary commensurate with industry standards for entry-level professional roles (Estimated range: ₹3.0 – ₹4.5 LPA).

Why This Role?

This position is specifically designed for candidates who wish to leverage their scientific background in a professional, office-based environment rather than a traditional QC laboratory. If you are analytical, process-driven, and looking to transition into the clinical data operations sector, this role provides the training and visibility necessary to excel in the global clinical research landscape.

How to Apply

Interested and qualified candidates are encouraged to submit their applications through the official Labcorp careers portal.

Click here to view the job posting and apply on the official Labcorp portal

Please ensure your application is submitted before the deadline of March 27, 2026.