CLINICAL PUBLISHING COORDINATOR
Company: Labcorp
Location: Bangalore, Karnataka, India
Department: Clinical Operations / Clinical Publishing
Job Type: Full-Time
Work Mode: On-Site
Shift: Rotational Shift
JOB OVERVIEW
Labcorp is seeking a Clinical Publishing Coordinator to support the preparation, management, and delivery of clinical trial documentation. The role involves creating and modifying investigator manuals, requisitions, and study-related documents, ensuring timely language translations, and maintaining high-quality project documentation in compliance with clinical research standards.
KEY RESPONSIBILITIES
Clinical Documentation Management
Create and modify Clinical Investigator Manuals (CIMs).
Prepare requisitions and other project-related documentation.
Ensure all documentation meets Study Scope of Work (SOW) requirements.
Deliver high-quality documentation within project timelines.
Maintain document accuracy, consistency, and compliance.
Clinical Publishing Support
Support the preparation and publishing of study-related materials.
Ensure documentation is complete and ready for distribution.
Coordinate document updates and revisions as required.
Assist in maintaining clinical publishing standards and procedures.
Translation Coordination
Track and coordinate language translations of study documents.
Ensure translated documents are completed within project timelines.
Collaborate with translation vendors and internal stakeholders when required.
Quality & Compliance
Follow departmental Standard Operating Procedures (SOPs).
Adhere to Work Instructions and internal guidelines.
Complete all mandatory training within required timelines.
Ensure quality and productivity targets are consistently achieved.
Escalate issues and risks in a timely manner.
Team Collaboration
Work closely with peers to ensure successful document delivery.
Support project teams in meeting documentation deadlines.
Participate in process improvement initiatives when required.
Perform additional responsibilities assigned by management.
EDUCATIONAL QUALIFICATIONS
Required
Bachelor’s Degree in Science
Preferred
Master’s Degree in Science
Life Sciences
Biotechnology
Microbiology
Biochemistry
Pharmacy
Clinical Research-related disciplines
EXPERIENCE
Required
Freshers can apply
Preferred
6 months or more experience in:
Clinical Research
CRO Industry
Clinical Documentation
Clinical Operations
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