Novo Nordisk Hiring Medical Writers | M.Pharm & Pharm.D Apply
Looking for a Medical Writer Job in the pharmaceutical industry? Here’s an excellent Pharma Job opportunity from Novo Nordisk for the position of Medical Writer in Bangalore, Karnataka. Candidates with M.Pharm, Pharm.D, along with relevant regulatory medical writing experience, are encouraged to apply. If you are looking to build your career in clinical development and regulatory documentation, don’t miss this exciting opportunity with one of the world’s leading healthcare companies.
- Job Title: Medical Writer
- Category: Clinical Development
- Location: Bangalore, Karnataka, IN
About the Company
Novo Nordisk is a globally recognized healthcare company with over 100 years of excellence in developing innovative treatments for chronic diseases. The company is committed to scientific innovation, quality, and improving patient lives worldwide. This Medical Writer Job offers professionals an opportunity to contribute to global clinical development programs while building a rewarding Pharma Job career.
Job Description
Novo Nordisk is hiring a Medical Writer to support its Clinical Reporting team. The selected candidate will prepare high-quality regulatory and clinical documents supporting global clinical development programs.
The role involves preparing Protocols, Clinical Trial Reports (CTRs), Investigator Brochures (IB), CTD Module 2 summaries, clinical submission documents, and regulatory response documents (Q&A). The candidate will collaborate with global stakeholders, represent Clinical Reporting in project discussions, and contribute to regulatory submissions while maintaining high-quality documentation standards.
Key Responsibilities
- Prepare Protocols, Clinical Trial Reports (CTRs), Investigator Brochures (IB), CTD Module 2 summaries, and regulatory response documents.
- Deliver high-quality medical writing documents within project timelines.
- Implement project strategies into clinical reporting documents.
- Collaborate with cross-functional stakeholders.
- Ensure alignment with Clinical Reporting strategy.
- Support continuous process improvements.
- Mentor team members and contribute to knowledge-sharing initiatives.
- Maintain compliance with global regulatory requirements.
- Represent Clinical Reporting in project teams.
Qualifications
Candidates should possess:
- PhD, Medical Degree, MSc, M.Pharm, Pharm.D, or equivalent qualification.
- Minimum 2 years of experience in regulatory medical writing.
- Experience with scientific writing in the pharmaceutical industry.
- Strong analytical and project management skills.
- Excellent written and spoken English.
- Ability to communicate complex scientific information clearly.
- Strong collaboration and stakeholder management skills.
- Quality-focused mindset with a continuous learning attitude.
How to Apply?
Interested candidates should submit their application online through the Novo Nordisk careers portal by uploading their updated CV. Applicants are encouraged to include a brief motivation statement within their resume.
- Application Deadline: 20 July 2026
