Labcorp Clinical Publishing Associate Jobs
- Labcorp Hiring Clinical Publishing Associate in Bangalore | Clinical Research Jobs Apply Now
- Company Overview
- Job Role & Responsibilities
- Clinical Publishing & Documentation
- Regulatory & Compliance Support
- Cross-Functional Coordination
- Process Improvement & Quality Assurance
- Eligibility / Qualifications
- Educational Qualification:
- Experience:
- Skills Required:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- What does a Clinical Publishing Associate do?
- Who is eligible for this role?
- Is experience mandatory?
- What skills are important?
- Does this role involve shifts?
Labcorp Hiring Clinical Publishing Associate in Bangalore | Clinical Research Jobs Apply Now
Labcorp is actively hiring for the position of Clinical Publishing Associate in its Clinical Research and Documentation team based in Bangalore. This full-time opportunity is ideal for candidates with around 2 years of experience in the clinical research industry who are looking to build a career in clinical trial documentation, publishing, and regulatory support.
This role is part of Labcorp’s global clinical development operations, where professionals contribute to high-quality clinical documentation, regulatory submission readiness, and efficient clinical trial execution.
Company Overview
Labcorp is a global leader in life sciences and healthcare services, providing comprehensive drug development solutions, diagnostic services, and clinical trial support to pharmaceutical and biotechnology companies worldwide. With a strong presence across multiple countries, Labcorp plays a critical role in accelerating drug development and improving patient outcomes.
The organization is known for its data-driven approach, advanced laboratory capabilities, and commitment to quality, compliance, and innovation in clinical research.
Job Role & Responsibilities
Clinical Publishing & Documentation
- Create, review, and modify clinical investigator manuals, requisition forms, and study-related documents
- Ensure timely delivery of project documentation aligned with study requirements and protocols
- Perform quality control (QC) checks on clinical documents and translations
Regulatory & Compliance Support
- Follow Standard Operating Procedures (SOPs), Work Instructions, and departmental guidelines
- Ensure documentation meets regulatory and client expectations
- Support audit readiness and compliance processes
Cross-Functional Coordination
- Collaborate with internal teams to ensure smooth documentation workflows
- Coordinate language translation activities for global clinical projects
- Ensure timely issue escalation and resolution
Process Improvement & Quality Assurance
- Participate in process improvement initiatives within the department
- Maintain high productivity and quality standards
- Complete assigned tasks within defined timelines
Eligibility / Qualifications
Educational Qualification:
Bachelor’s Degree in Science
Relevant Courses: B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, M.Sc Life Sciences, Clinical Research, Pharmaceutical Sciences
Experience:
- Minimum 2 years of experience in clinical research or related field
Skills Required:
- Strong attention to detail and documentation skills
- Knowledge of clinical research processes and documentation standards
- Good communication and interpersonal skills
- Ability to work in rotational shifts and manage timelines
- Proficiency in MS Office and clinical tools
Location & Salary
- Job Location: Bangalore (Yeshwanthpur – Brigade Twin Towers)
- Work Mode: Onsite
- Salary: Not disclosed (as per industry standards)
Application Process
Interested candidates can apply directly through the official Labcorp careers page:
Apply Here: https://careers.labcorp.com/global/en/job/2610882
Frequently Asked Questions (FAQs)
What does a Clinical Publishing Associate do?
The role focuses on preparing and managing clinical trial documents, ensuring compliance with regulatory standards.
Who is eligible for this role?
Candidates with a science degree and around 2 years of clinical research experience.
Is experience mandatory?
Yes, relevant experience in clinical research or documentation is required.
What skills are important?
Attention to detail, documentation accuracy, and knowledge of clinical trial processes.
Does this role involve shifts?
Yes, rotational shifts may be required.
| Category | Details |
|---|---|
| Company | Labcorp |
| Vacancies | Clinical Publishing Associate |
| Required Education | B.Sc, M.Sc Life Sciences |
| Experience | 2 Years Clinical Research Experience |
To apply for this job please visit careers.labcorp.com.
