Full Time

Regulatory Medical Writing

Myriad Consulting
Mumbai / Pune
₹3 - ₹16 LPA
Posted 06/02/2026

About the Role

Role & Responsibilities
• Prepare and review regulatory clinical documents for global submissions
• Develop Protocols, Clinical Study Reports (CSR), Clinical Study Pharmacology Reports, and Narratives
• Draft and review post-approval and lifecycle management documents
• Ensure compliance with regulatory guidelines and internal quality standards
• Collaborate with cross-functional teams across therapeutic areas
• Manage timelines and deliverables for assigned medical writing projects

Qualification
• Life Sciences graduate or postgraduate
• Relevant certification in medical or regulatory writing preferred

Experience
• 3.5 to 10 years of experience in Regulatory Medical Writing
• Hands-on experience with clinical and regulatory documentation

Skills
• Strong expertise in regulatory medical writing
• Excellent scientific writing and data interpretation skills
• Knowledge of global regulatory submission requirements
• Attention to detail and quality-focused mindset
• Ability to work in a fast-paced, office-based environment

CTC Range
• Suitable for candidates with current CTC between ₹3 – ₹16 LPA

Selection Process
• Interview

About the Company
• A professional consulting organisation delivering regulatory and medical writing services Supports global regulatory submissions across multiple therapeutic areas Focused on quality, compliance, and scientific excellence.

How to Apply
• Share your updated resume via email
• Email: consultingmyriad@gmail.com
• Subject line: Regulatory Medical Writing

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Regulatory Medical Writing at Myriad Consulting | Jobslly