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Labcorp Hiring Clinical Publishing Coordinator & Support I

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Labcorp is actively hiring for Clinical Publishing Coordinator and Coordinator Support I roles in Bengaluru, India. These positions are ideal for B.Sc / M.Sc Life Sciences graduates looking to enter the clinical research and drug development domain.

With increasing demand in clinical trial documentation, publishing, and regulatory support, these roles offer a strong entry point into the CRO (Contract Research Organization) industry.

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๐Ÿ” Job Overview

  • Company: Labcorp
  • Location: Bangalore (Yeshwanthpur โ€“ Brigade Twin Towers)
  • Role 1: Clinical Publishing Coordinator
  • Role 2: Coordinator Support I
  • Job Type: Full-time
  • Work Mode: Office-based (Rotational shifts)
  • Experience: Freshers / 0โ€“6 months preferred
  • Qualification: Bachelorโ€™s or Masterโ€™s Degree in Science

๐Ÿ“‹ Key Responsibilities

  • Follow SOPs (Standard Operating Procedures) and internal guidelines
  • Create and modify clinical investigator manuals, requisitions, and documentation
  • Ensure timely completion of clinical publishing deliverables
  • Coordinate language translations for study documents
  • Maintain quality and compliance standards in clinical documentation
  • Collaborate with internal teams for on-time project delivery
  • Escalate issues proactively to management
  • Manage multiple tasks with accuracy and attention to detail

๐ŸŽ“ Qualifications & Skills

Minimum Requirements:

  • Bachelorโ€™s Degree in Life Sciences (B.Pharm, BSc, etc.)

Preferred:

  • 0โ€“6 months experience in clinical research / pharmacovigilance / documentation
  • Masterโ€™s Degree (M.Pharm, MSc)

Core Skills:

  • Strong attention to detail
  • Good communication and documentation skills
  • Ability to multitask under deadlines
  • Basic understanding of clinical trial processes
  • Proficiency in MS Office tools

๐Ÿ’ผ Salary & Benefits

  • Estimated Salary: โ‚น2.8 LPA โ€“ โ‚น4.5 LPA
  • Exposure to global clinical trials and regulatory documentation
  • Structured training and onboarding programs
  • Opportunity to transition into roles like:
    • Clinical Data Management
    • Regulatory Affairs
    • Medical Writing

๐Ÿš€ Why This Role is Important

The Clinical Publishing Coordinator role is crucial in ensuring that clinical trial documents are accurate, compliant, and submission-ready. This is a high-demand function in CROs, especially with increasing global clinical research activities.


๐Ÿ“ How to Apply

Application Link for Clinical Publishing

Application Link for Support Roles

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