Novo Nordisk Medical Writer Job | M Pharm, PharmD Candidates Eligible
Looking for a Medical Writer Job in the pharmaceutical industry? Novo Nordisk is hiring Medical Writers in Bangalore for its Clinical Reporting team. This Novo Nordisk Career opportunity is ideal for M.Pharm, PharmD, PhD, and medical professionals with experience in regulatory medical writing and clinical documentation. Candidates will contribute to global clinical development programs by preparing clinical study reports, regulatory submission documents, investigator brochures, and other scientific content that supports drug development and regulatory approvals.
- Job Title: Medical Writer
- Location: Bangalore, Karnataka
About the Company
Novo Nordisk is a leading global healthcare company with more than 100 years of experience in developing innovative medicines and solutions for chronic diseases. The company focuses on improving patient outcomes through research, clinical development, and scientific innovation.
Job Description
This Medical Writer Job involves preparing high-quality clinical and regulatory documents to support global clinical development programs. Professionals joining through this Novo Nordisk Career opportunity will work closely with cross-functional teams to create scientific content, clinical reports, regulatory submissions, and trial-related documentation while ensuring compliance with global regulatory requirements.
Key Responsibilities
- Prepare clinical study reports, protocols, IBs, and regulatory documents.
- Develop CTD summaries and regulatory response documents.
- Coordinate with cross-functional teams and stakeholders.
- Support project discussions and strategic decisions.
- Ensure high-quality medical writing deliverables.
- Maintain regulatory compliance and support process improvements.
- Contribute to training and knowledge-sharing initiatives.
Qualifications & Experience
- Education: PhD or M Pharm, PharmD degree
- Experience:
- Minimum 2 years of experience in regulatory medical writing.
- Experience in scientific and clinical document preparation.
- Pharmaceutical industry experience preferred.
Required Skills
- Regulatory medical writing and clinical documentation expertise.
- Knowledge of clinical reporting, submissions, and global regulations.
- Scientific data interpretation and communication.
- Strong analytical, project management, and stakeholder management skills.
- Ability to work independently and manage multiple priorities.
- Quality-focused and compliance-driven mindset.
Application Deadline: 19 June 2026
