Labcorp Hiring for Clinical Publishing Coordinator Role
Labcorp, a global leader in clinical research and life sciences services, is hiring for the role of Clinical Publishing Coordinator at its Bangalore location. This opportunity is ideal for B.Pharm and M.Pharm graduates with 0–2 years of experience who are looking to build a career in clinical documentation, regulatory publishing, and trial‑related document management.
The role focuses on supporting clinical publishing activities, including document formatting, quality checks, coordination with cross‑functional teams, and maintaining regulatory‑ready documentation within global clinical trial environments. Candidates will gain hands‑on exposure to clinical study documentation workflows and industry‑standard quality practices.
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🏢 About the Organization
Labcorp is a global life sciences organization that supports drug development, diagnostics, and clinical research services. The company works closely with pharmaceutical and biotechnology organizations to deliver data‑driven insights and regulated clinical solutions. Working at Labcorp allows professionals to gain experience in compliance‑driven environments, global documentation standards, and cross‑functional clinical teams.
📊 Position Overview
- Position: Clinical Publishing Coordinator
- Department: CDM
- Location: Bangalore
- Experience: 0-2 years
- Qualification: B.Pharm, M.Pharm
- Job Type: Full-Time
- Last Date of application: 30 March 2026
📋 Key Responsibilities– Clinical Publishing Coordinator
- SOP & Training Compliance: Follow all applicable departmental SOPs, Work Instructions, and guidelines.
- Complete all required training programs within defined timelines.
- Daily Task Execution: Perform day‑to‑day tasks with a strong focus on quality, accuracy, and productivity.
- Create, update, and modify clinical investigator manuals, requisitions, and related study documents in accordance with Scope of Work (SOW) requirements to ensure timely and high‑quality deliverables.
- Ensure language translations of assigned project documents are completed accurately and within required timelines.
- Work closely with peers and cross‑functional teams to support the delivery of complete and compliant clinical publishing documentation.
- Identify issues proactively and ensure timely escalation to management when required.
- Perform other duties assigned by management in support of departmental and project needs.
🎓 Required Qualification
Candidates applying for this role should meet the following criteria:
- Educational background in Life Sciences, Pharmacy, Biotechnology, or related fields
- Basic understanding of clinical research or documentation processes
- Strong attention to detail and organizational skills
- Willingness to work with structured publishing workflows
- Good written communication skills
🧠 Essential Skills
The following skills are important for success in this role:
- Knowledge of clinical documentation basics
- Familiarity with document formatting and publishing tools (preferred)
- Strong organizational and tracking skills
- Attention to detail and accuracy
- Ability to manage multiple tasks and timelines
- Good proficiency in MS Office tools (Word, Excel, PowerPoint)
⭐ Role Summary
The Clinical Publishing Coordinator role plays a key part in ensuring that clinical documents are prepared, organized, and published accurately. While the role may not involve direct medical writing, it provides valuable exposure to clinical trial documentation standards and regulatory publishing processes. This position serves as a strong entry point into clinical documentation, medical writing support, and regulatory publishing careers.
🎯 Suitable Candidates
This opportunity is suitable for:
- Fresh graduates interested in clinical documentation roles
- Candidates seeking entry into medical writing or clinical publishing
- Professionals with documentation or coordination experience
- Individuals aiming to work in regulated life sciences environments
📈 Career Opportunities
With experience and skill development, candidates can progress into roles such as:
- Senior Clinical Publishing Coordinator
- Clinical Documentation Specialist
- Medical Writing Support Associate
- Regulatory Publishing Specialist
Long‑term experience may also lead to roles in medical writing or regulatory documentation.
💰 Salary Insight
- Expected Salary: As per Labcorp company standards
Compensation varies based on experience, role responsibilities, and work model.
💡 Practical Tips
- Be prepared to explain your interest in clinical publishing
- Learn basics of clinical document types and formats
- Practice document formatting and version control concepts
- Highlight attention‑to‑detail and coordination skills in your resume
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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❓FAQ – Clinical Publishing Coordinator
1. Who can apply for the Clinical Publishing Coordinator role at Labcorp?
Candidates with a Bachelor’s degree or higher, including B.Pharm and M.Pharm graduates, with 0–2 years of experience are eligible to apply.
2. Is this role suitable for freshers?
Yes. This role is suitable for freshers and entry‑level professionals, especially those interested in clinical documentation and publishing operations.
3. What type of work does a Clinical Publishing Coordinator do?
The role involves preparing and updating clinical investigator manuals, requisitions, study documents, coordinating translations, performing quality checks, and supporting clinical publishing workflows.
4. Do I need prior experience in clinical publishing?
Prior experience is not mandatory. However, basic exposure to clinical research or documentation will be considered an advantage.
5. Will I work with SOPs and Work Instructions?
Yes. You will follow departmental SOPs, Work Instructions, and guidelines to ensure quality, consistency, and compliance.
