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Labcorp is inviting applications for the position of Clinical Publishing Coordinator in Bangalore, India. This role is ideal for life sciences and pharmaceutical professionals who want to work in clinical research documentation, regulatory publishing, and trial support. Candidates will contribute to creating and managing high-quality investigator manuals, requisitions, and study documents in compliance with SOPs and timelines.
If you are detail-oriented, quality-driven, and passionate about clinical publishing careers in India, this opportunity with a global leader in healthcare diagnostics and clinical research may be the right fit.
Key Responsibilities
As a Clinical Publishing Coordinator at Labcorp, you will:
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- Follow departmental SOPs, Work Instructions, and guidelines.
- Complete required training within specified timelines.
- Ensure day-to-day publishing tasks are completed with accuracy and productivity.
- Create and modify clinical investigator manuals, requisitions, and project-related documentation as per SOW requirements.
- Coordinate language translations of project documents to ensure timely completion.
- Work collaboratively with peers to deliver accurate documentation packages.
- Escalate issues promptly to management.
- Perform additional duties as assigned.
Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.
- Experience in clinical publishing, clinical research, or regulatory documentation preferred.
- Strong attention to detail, organizational skills, and ability to meet deadlines.
- Proficiency in MS Office and document management systems is a plus.
Benefits of Joining Labcorp
- Opportunity to work with a global CRO and healthcare leader.
- Inclusive workplace culture promoting diversity and equal opportunity.
- Professional growth through continuous training and exposure to global projects.
- Competitive salary and employee benefits.
Application Process
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