Regulatory Medical Writing
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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