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

- Solid 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).
- Strong attention to detail and organizational skills.

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