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Labcorp Hiring Clinical Publishing Coordinator | Freshers
Labcorp
Bangalore
0–2 Years
Clinical Publishing
Clinical Research
Full-Time
🏢 About Labcorp
Labcorp is a global life sciences and healthcare diagnostics company providing laboratory services, clinical development solutions, and drug development support to pharmaceutical and biotechnology organizations worldwide.
The company supports clinical trials, regulatory documentation, and healthcare research across multiple therapeutic areas, helping advance innovative treatments and improve patient outcomes.
📌 Job Overview
- Role: Clinical Publishing Coordinator
- Company: Labcorp
- Location: Bangalore, India
- Experience: 0–2 Years
- Qualification: B.Pharm / M.Pharm / Pharm.D / BSc / MSc Life Sciences
- Industry: Clinical Research / Regulatory Documentation
🔬 Key Responsibilities
- Follow departmental SOPs, work instructions, and publishing guidelines
- Complete mandatory training within required timelines
- Create and modify investigator manuals and project documentation
- Prepare clinical trial requisitions and regulatory publishing materials
- Coordinate language translations of study documentation
- Collaborate with internal teams to deliver accurate documentation packages
- Ensure publishing tasks meet productivity and quality targets
- Escalate documentation or project issues to management when needed
🎓 Eligibility Criteria
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- 0–2 years experience in clinical research or documentation
- Knowledge of clinical trial documentation is beneficial
- Good organizational and time management skills
💻 Required Skills
- Strong attention to detail
- Ability to manage documentation deadlines
- Knowledge of clinical research documentation workflows
- Proficiency in Microsoft Office tools
- Good communication and collaboration skills
🚀 Benefits of Working at Labcorp
- Work with a global clinical research and healthcare organization
- Exposure to international clinical trial documentation processes
- Structured training and professional development
- Opportunity to work with experienced clinical research teams
- Career growth in clinical publishing and regulatory documentation
🎯 Interview Preparation Tips
- Understand basics of clinical trial documentation
- Learn about Trial Master File (TMF) and regulatory documents
- Revise Good Clinical Practice (GCP) guidelines
- Practice document formatting and publishing workflows
- Review fundamentals of clinical research processes
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Make sure your qualifications and skills match the role requirements.
Kindly read the entire job description carefully before applying. Make sure your qualifications and skills match the role requirements.
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