Senior Medical Regulatory Writer
Sanofi is hiring a Senior Medical Regulatory Writer within their Business Operations team in Hyderabad. The role involves independently authoring and editing high-quality clinical and safety documents such as CSRs, PBRERs, and clinical evaluation reports. Candidates must possess expertise in regulatory writing, ICH/GCP/GVP standards, and scientific data interpretation. You will collaborate with global medical, pharmacovigilance, and regulatory teams to ensure audit-readiness and compliance.
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Experience
5+ years
Function
Research
Work mode
Onsite, India
Company
Tier 2
What you will work on
Sanofi is hiring a Senior Medical Regulatory Writer within their Business Operations team in Hyderabad. The role involves independently authoring and editing high-quality clinical and safety documents such as CSRs, PBRERs, and clinical evaluation reports. Candidates must possess expertise in regulatory writing, ICH/GCP/GVP standards, and scientific data interpretation. You will collaborate with global medical, pharmacovigilance, and regulatory teams to ensure audit-readiness and compliance.
TAL's take
Global pharma company offering a well-defined senior-level role in regulatory writing.
Clear expectations for document types, stakeholders, and regulatory standards to be managed.
Salaries at Sanofi
21.8 LPA average
Based on 8 Grapevine salary entries for Sanofi.
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Must haves
- 5+ years experience in regulatory writing for pharmaceuticals/healthcare industry
- Knowledge of ICH and GCP/GVP guidelines
- Technical medical editing and writing skills
- Data retrieval and scientific data interpretation skills
- Ability to work independently with minimal supervision
Tools and skills
About the company
Sanofi is a major global pharmaceutical company; assigned tier 2 as an established MNC.
Posts mentioning Sanofi
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