Remote Document Specialist Job in Global CRO (Parexel) – ₹9 LPA Salary | Medical Writing Support 2026

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Document Specialist I – Parexel | Remote Clinical Documentation Jobs in India

Parexel

Remote – India

3+ Years

Medical Writing Support

Full-Time

📄 Job Overview

Parexel, a globally recognized biopharmaceutical services company, is hiring Document Specialist I for its Medical Writing Support team.

This is a remote opportunity in India for professionals experienced in clinical document compilation, publishing, and regulatory submission formatting.

The role directly supports global clinical trials and regulatory deliverables that impact patient health worldwide.

📑 Role: Document Specialist I

Location: Remote – India

Eligible Cities: Mumbai, Hyderabad, Bengaluru, Chandigarh

Experience: Minimum 3 Years

Key Responsibilities:

• Compile appendices for Clinical Study Reports (CSRs)
• Coordinate with Medical Writers and Clinical Teams
• Apply MS Word formatting as per SOPs and regulatory standards
• Create submission-ready documents with hyperlinks and navigability
• Manage draft and final document distribution
• Perform QC checks to ensure submission readiness
• Ensure compliance with ICH and client SOPs
• Support timelines, approvals, and document workflows
• Maintain proper filing of project documentation

🧠 Required Skills

• Advanced MS Word & MS Office formatting
• Strong knowledge of Adobe Acrobat (PDF processing)
• Experience with publishing software & document management systems
• Ability to QC/format 15–17 pages per hour
• Knowledge of medical & pharmaceutical terminology
• Excellent communication and attention to detail

🎓 Education & Experience

• B.Pharm / M.Pharm / Pharm.D
• BSc / MSc – Life Sciences
• Health Sciences / Computer Science / Technology
• Experience in CSRs, submission dossiers, or regulatory documents
• Prior Document Technologist / Specialist experience preferred

💰 Salary (Estimated)

• ₹4,00,000 – ₹9,00,000 per annum
• As per industry standards & experience
• Global CRO exposure & long-term career growth

📌 Note Before You Apply:
Please read the full job description carefully before applying. Ensure your experience aligns with clinical documentation and regulatory publishing requirements.

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