Labcorp is actively hiring for Clinical Publishing Coordinator and Coordinator Support I roles in Bengaluru, India. These positions are ideal for B.Sc / M.Sc Life Sciences graduates looking to enter the clinical research and drug development domain.
With increasing demand in clinical trial documentation, publishing, and regulatory support, these roles offer a strong entry point into the CRO (Contract Research Organization) industry.
🔍 Job Overview
- Company: Labcorp
- Location: Bangalore (Yeshwanthpur – Brigade Twin Towers)
- Role 1: Clinical Publishing Coordinator
- Role 2: Coordinator Support I
- Job Type: Full-time
- Work Mode: Office-based (Rotational shifts)
- Experience: Freshers / 0–6 months preferred
- Qualification: Bachelor’s or Master’s Degree in Science
📋 Key Responsibilities
- Follow SOPs (Standard Operating Procedures) and internal guidelines
- Create and modify clinical investigator manuals, requisitions, and documentation
- Ensure timely completion of clinical publishing deliverables
- Coordinate language translations for study documents
- Maintain quality and compliance standards in clinical documentation
- Collaborate with internal teams for on-time project delivery
- Escalate issues proactively to management
- Manage multiple tasks with accuracy and attention to detail
🎓 Qualifications & Skills
Minimum Requirements:
- Bachelor’s Degree in Life Sciences (B.Pharm, BSc, etc.)
Preferred:
- 0–6 months experience in clinical research / pharmacovigilance / documentation
- Master’s Degree (M.Pharm, MSc)
Core Skills:
- Strong attention to detail
- Good communication and documentation skills
- Ability to multitask under deadlines
- Basic understanding of clinical trial processes
- Proficiency in MS Office tools
💼 Salary & Benefits
- Estimated Salary: ₹2.8 LPA – ₹4.5 LPA
- Exposure to global clinical trials and regulatory documentation
- Structured training and onboarding programs
- Opportunity to transition into roles like:
- Clinical Data Management
- Regulatory Affairs
- Medical Writing
🚀 Why This Role is Important
The Clinical Publishing Coordinator role is crucial in ensuring that clinical trial documents are accurate, compliant, and submission-ready. This is a high-demand function in CROs, especially with increasing global clinical research activities.
📝 How to Apply
Application Link for Clinical Publishing
Application Link for Support Roles
