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Clinical Publishing Coordinator

Labcorp
0.5-2 years
INR 3 LPA – 6 LPA
Bangalore, India
1 June 23, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

CLINICAL PUBLISHING COORDINATOR

Company: Labcorp
Location: Bangalore, India
Job ID: 2619045
Category: Clinical
Job Type: Full-Time
Work Mode: On-Site

JOB OVERVIEW

Labcorp is seeking a Clinical Publishing Coordinator to join its Clinical Operations team in Bangalore. The role involves creating and managing clinical study documentation, coordinating document publishing activities, supporting language translations, ensuring compliance with project requirements, and maintaining high-quality deliverables for global clinical research projects.

WORK SCHEDULE

  • Rotational Shift

  • Full-Time Position

KEY RESPONSIBILITIES

• Clinical Document Preparation

  • Create and modify Clinical Investigator Manuals.

  • Prepare requisitions and other project-related documentation.

  • Ensure documentation meets project Scope of Work (SOW) requirements.

  • Deliver accurate and high-quality clinical documents within timelines.

• Clinical Publishing Support

  • Support publication and distribution of clinical study documents.

  • Maintain document consistency and formatting standards.

  • Ensure project documentation is complete and compliant.

• Translation Coordination

  • Coordinate language translation activities for project documents.

  • Ensure translated documents are completed within project timelines.

  • Monitor translation quality and delivery schedules.

• Quality & Compliance

  • Follow departmental Standard Operating Procedures (SOPs).

  • Adhere to Work Instructions and departmental guidelines.

  • Complete mandatory training within required timelines.

  • Maintain quality standards in all deliverables.

• Project Coordination

  • Collaborate effectively with internal teams and stakeholders.

  • Work closely with peers to ensure timely project delivery.

  • Escalate issues and risks appropriately when required.

  • Support management with additional assigned responsibilities.

REQUIRED QUALIFICATIONS

  • Bachelor's Degree in Science

PREFERRED QUALIFICATIONS

  • Master's Degree in Science

  • 6 Months or more experience in:

    • Clinical Research

    • Clinical Operations

    • Pharmaceutical Industry

    • CRO Environment