Role & responsibilities
Prepare and review medical, scientific, and clinical documents including:
Clinical Study Reports (CSRs)
Protocols and Investigator Brochures
Regulatory submission documents
Standard Operating Procedures (SOPs)
Scientific manuscripts and publications
Medical education and training materials
Patient information leaflets and consent forms
Conduct literature reviews and summarize scientific findings.
Collaborate with cross-functional teams including Medical Affairs, Clinical Research, Regulatory Affairs, Pharmacovigilance, and Marketing.
Ensure all documents comply with regulatory and company guidelines.
Edit and proofread content for clarity, accuracy, consistency, and scientific integrity.
Support the preparation of presentations, abstracts, posters, and conference materials.
Maintain document version control and archive records as per compliance requirements.

Preferred candidate profile
Robust scientific and medical writing skills.
Excellent written and verbal communication skills in English.
Ability to interpret and summarize complex scientific data.
Proficiency in Microsoft Office (Word, PowerPoint, Excel).
Robust attention to detail and organizational skills.

📌 Medical Writer Udaipur (India)
🏢 Indira IVF Hospital
📍 India