Are you a wordsmith with a passion for science? Do you enjoy transforming complex clinical data into clear, regulatory-compliant documents? If yes, this opportunity at Meril Life Sciences could be your next big career move!
Whether you prefer working from the innovation hub of Ahmedabad or remotely, this role offers flexibility along with global exposure in the rapidly growing medical device industry.
As the pharmaceutical and medical device industries continue to evolve, the demand for high-quality scientific communication is at an all-time high. This role gives you the opportunity to work on impactful clinical documents that support life-saving innovations.
In this position, you will act as a bridge between scientific data and regulatory requirements—ensuring accuracy, compliance, and clarity across all documentation while collaborating with cross-functional teams globally.
📩 How to Apply
If you are ready to elevate your career in clinical research and medical writing, Meril Life Sciences wants to hear from you!
📧 Send your updated resume to: rahulkumar.cr@merillife.com
📝 Subject Line: Application for Medical Writer – [Your Name] – [Years of Experience]
🌟 Role Overview: Bridging Science & Regulatory Excellence
As a Medical Writer / Clinical Researcher, you’ll play a crucial role in converting scientific data into high-quality documentation that supports clinical trials and regulatory submissions.
✍️ Key Responsibilities
1. Core Clinical Documentation
- Clinical Study Protocols
- Informed Consent Forms (ICF)
- Clinical Study Reports (CSR)
- Standard Operating Procedures (SOPs)
2. Scientific Writing & Publications
- Manuscripts, white papers, literature reviews
- Plain language summaries
- Conference abstracts
3. Regulatory Compliance
Work in alignment with:
- ICH-GCP guidelines
- Food and Drug Administration
- European Medicines Agency
- Pharmaceuticals and Medical Devices Agency
- Indian Council of Medical Research
4. Data Interpretation
- Literature reviews
- Clinical data analysis
- Training material support
5. Collaboration
- Clinical teams
- Biostatisticians
- Regulatory & safety teams
🎯 Candidate Profile
- Degree in Life Sciences / Pharmacy / Medicine / Biotechnology
- 3–5 years of experience in medical writing
- Strong analytical and documentation skills
- Attention to detail and regulatory understanding
⭐ Why Join Meril Life Sciences?
- Global exposure
- Career growth opportunities
- Flexible work setup (Remote/Ahmedabad)
- Work with industry experts
