Medical Regulatory Writer at Sanofi Job – Apply Now!
- Write and edit high-quality safety and medical documents, including Periodic Benefit-Risk Evaluation Reports (PBRER), Addendums to Clinical Overviews (ACO), Disease and Product ID Cards, Product Alerts, and Trial Transparency Documents.
- Deliver medical documents in compliance with internal and external standards.
- Maintain effective relationships with stakeholders.
- Assist other medical regulatory writers in developing knowledge.
Performance:
- Provide deliverables as per agreed timelines and quality.
Process:
- Author, review, and act as an expert in medical regulatory writing.
Stakeholders:
- Work closely with clinical/medical teams to identify writing needs.
- Education: Advanced degree in life sciences/pharmacy or medical degree
- Soft skills: Stakeholder management; communication skills; ability to work independently and within a team environment
- Technical skills: Excellent technical editing and writing skills; knowledge of scientific data interpretation
- Experience: For Medical Regulatory Writer Job >2 years in regulatory writing for the pharmaceuticals/healthcare industry
- Languages: Excellent English language knowledgeAPPLY ONLINE HERE
Keywords: Medical Regulatory Writer, Sanofi, Hyderabad, India, Pharmaceutical Industry, Healthcare, Regulatory Writing
