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).

- Strong attention to detail and organizational skills.

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