Parexel Hiring Medical Writing Support Coordinator | Remote Medical Writing Jobs India 2026

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Parexel Hiring Medical Writing Support Coordinator | Remote Medical Writing Jobs India 2026

✔ Verified by Medical Jobs India

Parexel Hiring Medical Writing Support Coordinator | Remote India

🏢 Parexel
📍 Bengaluru & Mohali
🌍 Remote India
🧪 Medical Writing
🎓 Life Sciences & Pharmacy

Parexel is hiring Medical Writing Support Coordinators (MWSC) for remote opportunities in India.

This role is ideal for candidates interested in Medical Writing, Clinical Documentation, Regulatory Support, Clinical Research Operations, SharePoint Management, and CRO Careers.

📋 Job Overview

  • Company: Parexel
  • Role: Medical Writing Support Coordinator
  • Locations: Bengaluru & Mohali
  • Work Mode: Remote India
  • Job Type: Full-Time
  • Industry: Clinical Research / CRO / Medical Writing
  • Qualification: Life Sciences / Pharmacy / Biotechnology / Medical Field
💰 Expected Salary: ₹3.5 – ₹6.5 LPA

🏢 About Parexel

Parexel is a globally recognized Contract Research Organization (CRO) specializing in clinical research, regulatory consulting, medical writing, and clinical development services.

The company provides excellent opportunities for candidates looking to build careers in Medical Writing, Clinical Documentation, Regulatory Affairs, and Global Clinical Operations.

📌 Key Responsibilities

📂 Project Filing & Documentation

  • Organize and maintain clinical and regulatory documents
  • Ensure proper document version control and archiving
  • Maintain structured filing systems for deliverables

✍️ Medical Writing Project Support

  • Support medical writers in documentation workflows
  • Assist with project coordination and communication
  • Manage project files and tracking timelines

📊 Administrative & Coordination Tasks

  • Schedule meetings and prepare meeting minutes
  • Maintain project trackers and reporting logs
  • Support administrative and coordination activities

🧪 Advanced Documentation Support

  • Prepare QC document packages
  • Support inspection readiness activities
  • Manage SharePoint folders and review workflows
  • Assist in regulatory document submissions

🎓 Eligibility Criteria

Eligible Qualifications

  • Life Sciences
  • Pharmacy
  • Biotechnology
  • Medical Field Backgrounds

⭐ Required Skills

  • Strong interest in Medical Writing and Clinical Research
  • MS Office and documentation management skills
  • SharePoint knowledge preferred
  • Excellent written and verbal communication
  • Ability to manage confidential clinical data
  • Strong organizational and multitasking abilities
  • Ability to work independently

➕ Additional Advantage

  • IT or documentation-related skills
  • Clinical documentation exposure
  • Project coordination experience

🚀 Why This Role is High-Value for Your Career

This Medical Writing Support Coordinator role provides an excellent pathway into:

  • Medical Writer / Scientific Writer
  • Regulatory Writing Specialist
  • Clinical Documentation Specialist
  • Pharmacovigilance & Safety Writing
  • Clinical Research Operations

Working with Parexel offers strong global exposure to clinical documentation workflows, QC processes, and regulatory submission standards used across the pharmaceutical industry.

🌍 Benefits of Working at Parexel

  • Remote work flexibility across India
  • Career growth in Medical Writing & Regulatory Support
  • Exposure to global clinical research projects
  • Collaborative international work environment
  • Structured learning and development opportunities
  • Opportunity to work with global clients and teams

📄 Resume & Interview Tips

  • Highlight documentation and coordination skills
  • Mention MS Office and SharePoint knowledge
  • Add clinical research or regulatory exposure
  • Showcase written communication abilities
  • Keep resume ATS-friendly and professional

🚀 Job Application Link

📌 Important Note Before You Apply:

Please make sure to read the complete job description carefully before submitting your application. Make sure your Medical Writing, Documentation, and Clinical Research interests align with the role requirements before proceeding.
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