Labcorp Hiring Clinical Publishing Coordinator (Freshers / 0–2 Years)
Are you seeking high-paying Labcorp Clinical Publishing Coordinator Jobs or Clinical Publishing Careers in Bangalore? Labcorp, a premier global life sciences and clinical research organization (CRO), has announced an exciting vacancy for a Clinical Publishing Coordinator based at its regional office in Yeshwanthpur, Bangalore.
This role is perfect for freshers and early-career professionals from biotechnology, pharmacy, or biological background who want to build a career in clinical study documentation, quality assurance workflows, and regulatory affairs administration. To prepare your profile and application, you can read our detailed instructions on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Clinical Publishing Coordinator |
| Company | Labcorp (Clinical Research Services) |
| Job ID | 2619045 |
| Location | Yeshwanthpur, Bengaluru, Karnataka, India |
| Employment Type | Full-Time |
| Work Mode | Rotational Shift |
| Experience Required | 0–2 Years (Freshers with 6 months internship preferred) |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc & M.Sc in Life Sciences, Biotechnology |
| Application Deadline | June 26, 2026 (Apply Immediately) |
💼 Key Responsibilities
- Prepare, format, and modify clinical investigator manuals, project documentation, and laboratory requisitions.
- Ensure clinical trial documentation and deliverables (DP documentation) meet global submission timelines and quality requirements.
- Coordinate and manage translation processes of patient-facing and clinical investigator materials.
- Adhere strictly to standard operating procedures (SOPs), safety protocols, and regulatory guidelines in a CRO environment.
- Collaborate actively with global clinical operations coordinators, study start-up personnel, and biostatisticians.
- Participate in internal audits and complete documentation workflows with high accuracy and productivity.
- Proactively identify and escalate document discrepancies or delivery issues to project leads.
Clinical publishing is closely integrated with clinical data workflows. To test your knowledge of clinical trials, try out our Clinical Trial Assistant (CTA) Quiz.
🎓 Eligibility Criteria & Qualifications
Candidates should meet the following educational standards:
- Minimum: Bachelor's Degree in Pharmacy (B.Pharm), Biotechnology (B.Tech / B.Sc), or other related Life Sciences fields.
- Preferred: Master's Degree (M.Pharm / M.Sc) in Biotechnology or Life Sciences.
- Candidates with at least 6 months of experience in clinical documentation or healthcare publishing will hold a distinct advantage.
For pharmacy graduates mapping out long-term career routes, read our comparisons on B.Pharm Careers: India vs USA.
Required Core Skills
- Meticulous attention to detail (critical for reviewing large-scale clinical manuals and documents).
- Effective written and verbal communication skills in English.
- Strong organizational and multitasking skills with the capability to meet tight project timelines.
- Basic understanding of drug development phases, clinical trial documentation, and ICH-GCP rules.
- Adaptability to rotating shift patterns in a global clinical research ecosystem.
💰 Salary & Compensation
Selected candidates will receive:
- Salary Package: ₹3.5 LPA – ₹6.0 LPA (Estimated, based on experience and benchmarks).
- Corporate benefits including health insurance, shift allowance, and transport assistance.
- Exposure to global clinical trial platforms and professional development opportunities.
If you are evaluating your skills for core clinical roles vs tech administration, read our analysis on Healthcare IT vs Clinical Healthcare.
🌟 Why Join Labcorp?
- Labcorp is a global leader in diagnostics and clinical drug development operations.
- Provides a massive learning curve to transition into Medical Writing, Regulatory Affairs, or Clinical Trial Management.
- Collaborative and diverse workplace implementing the highest quality and scientific standards.
To learn about roles related to documentation in global clinical studies, read our Clinical Research Coordinator (CRC) Guide.
📑 Resume Tips for Labcorp
- Highlight any specific training, projects, or internships related to medical documentation or regulatory guidelines.
- List your proficiency in document review, formatting tools, and clinical trial knowledge.
- Clearly state your availability to work in rotating shifts at Yeshwanthpur, Bangalore.
- Ensure your CV is clean, professional, and optimized for Applicant Tracking Systems (ATS).
🎯 Labcorp Interview Questions
- What are the core components of a Clinical Investigator Manual?
- How do you ensure error-free formatting when reviewing large clinical study documents under tight timelines?
- What is your understanding of standard operating procedures (SOPs) and why are they critical in clinical publishing?
- Can you explain the difference between Phase II and Phase III clinical trials?
- Are you comfortable working in a rotating shift schedule to align with global project requirements?
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through Labcorp's Workday portal using the link below. Ensure you submit your application before the deadline on June 26, 2026. For guidance on optimizing your application profile, read our tutorial on how to apply for healthcare and pharma jobs.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. When is the application deadline?
The portal closes on June 26, 2026.
Q. Who is eligible for this role?
B.Pharm, M.Pharm, Pharm.D, B.Sc & M.Sc (Life Sciences/Biotechnology) graduates with 0-2 years of experience.
Q. What is the work location and mode?
The role is full-time based at Labcorp's offices in Brigade Twin Towers, Yeshwanthpur, Bangalore, operating in rotational shifts.
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