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Coordinator Support I

Labcorp
Fresher years
Not Disclosed
Bangalore, India
1 June 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Coordinator Support I (Clinical Publishing Coordinator)

Company: Labcorp
Location: Bangalore, Karnataka, India
Department: Clinical Operations / Clinical Publishing
Job Type: Full-Time (Office-Based)
Work Schedule: Rotational Shift


Role Summary

The Coordinator Support I (Clinical Publishing Coordinator) is responsible for supporting clinical documentation and publishing activities by creating, modifying, and maintaining investigator manuals, requisitions, and other project-related materials. The role ensures timely delivery of accurate clinical documents, coordinates translation activities, and supports compliance with project requirements, SOPs, and quality standards.


Key Responsibilities

Clinical Documentation & Publishing

  • Create and update Clinical Investigator Manuals, requisitions, and other project-related documentation.

  • Ensure all clinical publishing deliverables are completed according to Study Work Order (SOW) requirements.

  • Maintain document accuracy, consistency, and quality throughout the publication process.

  • Support preparation and maintenance of project documentation required for clinical studies.

Translation Coordination

  • Coordinate language translation activities for assigned project documents.

  • Ensure translated materials are completed accurately and delivered within project timelines.

  • Monitor translation status and follow up with relevant stakeholders as required.

Project Support

  • Complete assigned day-to-day operational tasks while maintaining productivity and quality standards.

  • Work collaboratively with team members to ensure timely delivery of documentation packages.

  • Support project execution by adhering to departmental procedures and timelines.

  • Escalate issues, risks, or delays to management in a timely manner.

Compliance & Quality Management

  • Follow departmental Standard Operating Procedures (SOPs), Work Instructions (WIs), and internal guidelines.

  • Complete all mandatory training programs within required timelines.

  • Ensure compliance with quality standards and documentation requirements.

  • Contribute to maintaining inspection-ready and audit-compliant documentation.


Required Qualifications

Education

  • Bachelor’s Degree in Science.

Experience

  • Freshers can apply.

  • Clinical research experience is not mandatory.


Preferred Qualifications

Education

  • Master’s Degree in Science.

Experience

  • Minimum 6 months of experience in Clinical Research or related industry.