Labcorp Hiring for Clinical Publishing Coordinator Role

ByPharma Hiring Hub

Labcorp, a global leader in clinical research and life sciences services, is hiring for the role of Clinical Publishing Coordinator at its Bangalore location. This opportunity is ideal for B.Pharm and M.Pharm graduates with 0–2 years of experience who are looking to build a career in clinical documentation, regulatory publishing, and trial‑related document management.

The role focuses on supporting clinical publishing activities, including document formatting, quality checks, coordination with cross‑functional teams, and maintaining regulatory‑ready documentation within global clinical trial environments. Candidates will gain hands‑on exposure to clinical study documentation workflows and industry‑standard quality practices.

This position offers a strong entry‑level opportunity to develop long‑term expertise in clinical publishing and regulatory documentation within a globally recognized CRO.

Labcorp career

Job Overview

  • Position: Clinical Publishing Coordinator
  • Department: CDM
  • Location: Bangalore
  • Experience: 0-2 years
  • Qualification: B.Pharm, M.Pharm
  • Job Type: Full-Time
  • Last Date of application: 30 March 2026

Key Responsibilities – Clinical Publishing Coordinator

  • SOP & Training Compliance: Follow all applicable departmental SOPs, Work Instructions, and guidelines.
  • Complete all required training programs within defined timelines.
  • Daily Task Execution: Perform day‑to‑day tasks with a strong focus on quality, accuracy, and productivity.
  • Clinical Document Preparation: Create, update, and modify clinical investigator manuals, requisitions, and related study documents in accordance with Scope of Work (SOW) requirements to ensure timely and high‑quality deliverables.
  • Translation & Publishing Coordination: Ensure language translations of assigned project documents are completed accurately and within required timelines.
  • Team Collaboration: Work closely with peers and cross‑functional teams to support the delivery of complete and compliant clinical publishing documentation.
  • Issue Escalation: Identify issues proactively and ensure timely escalation to management when required.
  • Additional Responsibilities: Perform other duties assigned by management in support of departmental and project needs.

Required Skills & Qualifications

  • Educational Background: Bachelor’s degree or above in a relevant discipline.
  • Core Skills
    • Demonstrated ability to organize tasks and communicate effectively.
    • Strong attention to detail with a focus on accuracy and documentation quality.
    • Ability to work collaboratively with team members and stakeholders.
    • Consistent delivery of high‑quality work outputs within defined timelines.
    • Comfortable using computer systems and departmental tools.
  • Clinical Research Knowledge: Basic understanding of clinical research processes and clinical documentation workflows.
  • Work Environment
    • Role is performed in a general office setting.
    • Requires the ability to work for extended periods at a computer workstation.
  • Workload & Flexibility
    • Ability to perform effectively with multiple interruptions.
    • Capable of managing multiple priorities simultaneously.
    • May require overtime based on project and business needs.

Why Join Labcorp

  • Structured Work Environment
  • Work within well‑defined SOPs, Work Instructions, and quality standards, ensuring accuracy, compliance, and audit‑ready documentation.
  • Collaborative Team Culture
  • Collaborate with cross‑functional teams and peers in a professional and supportive environment focused on timely and high‑quality deliverables.
  • Skill Development & Learning
  • Develop strong skills in documentation management, quality checks, workflow coordination, and clinical publishing tools, supporting long‑term career growth.
  • Career Progression Paths
  • Build a foundation for future roles in Clinical Publishing, Regulatory Documentation, Clinical Operations, or broader life sciences functions.
  • Meaningful Contribution
  • Your work supports clinical trial conduct and regulatory readiness, contributing to the advancement of safe and effective medicines globally.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ – Clinical Publishing Coordinator

1. Who can apply for the Clinical Publishing Coordinator role at Labcorp?

Candidates with a Bachelor’s degree or higher, including B.Pharm and M.Pharm graduates, with 0–2 years of experience are eligible to apply.

2. Is this role suitable for freshers?

Yes. This role is suitable for freshers and entry‑level professionals, especially those interested in clinical documentation and publishing operations.

3. What type of work does a Clinical Publishing Coordinator do?

The role involves preparing and updating clinical investigator manuals, requisitions, study documents, coordinating translations, performing quality checks, and supporting clinical publishing workflows.

4. Do I need prior experience in clinical publishing?

Prior experience is not mandatory. However, basic exposure to clinical research or documentation will be considered an advantage.

5. Will I work with SOPs and Work Instructions?

Yes. You will follow departmental SOPs, Work Instructions, and guidelines to ensure quality, consistency, and compliance.

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