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Looking to build a career in clinical research documentation, clinical publishing, and regulatory documentation workflows? Labcorp is hiring a Clinical Publishing Coordinator in Bangalore, offering a strong entry-level opportunity for candidates from Pharmacy and Biotechnology backgrounds.
This role is ideal for candidates interested in clinical trial documentation, investigator manuals, and publishing operations in CRO environments.
📍 Job Overview
- Job Title: Clinical Publishing Coordinator
- Location: Bangalore, Karnataka (Brigade Twin Towers, Yeshwanthpur)
- Employment Type: Full-time
- Work Mode: Rotational Shift
- Experience: 0–1 year (Freshers + 6 months experience preferred)
- Last Date to Apply: April 3, 2026
🧩 Key Responsibilities
As a Clinical Publishing Coordinator, you will be responsible for:
- Preparing and modifying clinical investigator manuals, requisitions, and project documentation
- Ensuring clinical publishing deliverables (DP documentation) meet timelines and quality standards
- Managing language translations of clinical trial documents
- Following SOPs, Work Instructions, and compliance guidelines
- Coordinating with cross-functional teams for clinical documentation workflows
- Completing assigned tasks with high accuracy, productivity, and compliance
- Escalating issues proactively to ensure smooth project delivery
🎓 Qualifications
✅ Minimum:
- Bachelor’s Degree in Pharmacy / Biotechnology / Life Sciences
⭐ Preferred:
- 6 months+ experience in clinical research / clinical documentation
- Master’s Degree in Biotechnology or related field
🧠 Required Skills
- Strong attention to detail (critical for clinical publishing roles)
- Good communication and documentation skills
- Ability to manage multiple priorities and deadlines
- Understanding of clinical trial processes and documentation standards
- Team collaboration and adaptability in a CRO environment
💰 Salary (Estimated)
- ₹3.5 LPA – ₹6 LPA (based on experience and industry benchmarks for entry-level clinical publishing roles in Bangalore)
🌟 Why Join Labcorp?
- Work with a global CRO leader in clinical trials and diagnostics
- Exposure to clinical publishing, regulatory documentation, and trial workflows
- Strong learning curve for careers in:
- Clinical Data Management (CDM)
- Regulatory Affairs
- Medical Writing
- Pharmacovigilance documentation
- Inclusive and diverse workplace with global standards
📩 How to Apply
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