Novo Nordisk, one of the world’s leading pharmaceutical companies, has announced an exciting opportunity for experienced Medical Writers in Bangalore, Karnataka. Professionals with a background in Life Sciences, Pharmacy, Medicine, or related disciplines and at least two years of regulatory medical writing experience are encouraged to apply.

This Novo Nordisk Medical Writer Job 2026 offers an excellent opportunity to work with global clinical development teams, contribute to regulatory submissions, and prepare high-quality scientific documents supporting innovative therapies. Candidates looking for Medical Writer jobs in Bangalore, regulatory medical writing jobs, or pharmaceutical writing careers in India should not miss this opportunity.

Job Overview

About Novo Nordisk

Novo Nordisk is a globally recognized healthcare company with more than 100 years of experience in developing innovative treatments for chronic diseases. The company’s Clinical Reporting team plays a critical role in global drug development by delivering high-quality regulatory documents that support clinical trials and worldwide regulatory submissions.

Working at Novo Nordisk provides professionals with opportunities to collaborate across international teams while contributing to life-changing therapies.

Key Responsibilities

As a Medical Writer at Novo Nordisk, you will:

• Prepare clinical and regulatory documents including Protocols, Clinical Trial Reports (CTRs), Investigator Brochures (IBs), CTD Module 2 summaries, and regulatory response documents.
• Deliver high-quality clinical reporting documents aligned with global regulatory standards.
• Collaborate with cross-functional stakeholders across Clinical Development, Biostatistics, Regulatory Affairs, and Medical teams.
• Support clinical reporting strategies across development programs.
• Review scientific content for quality, consistency, and compliance.
• Participate in project discussions and represent the Clinical Reporting function.
• Contribute to process improvements and continuous quality initiatives.
• Mentor team members and support knowledge-sharing activities.
• Stay updated with international regulatory guidelines and medical writing best practices.

Eligibility Criteria

Applicants should possess:

• PhD, Medical Degree, MSc, M.Pharm, PharmD, or equivalent qualification.
• Minimum 2 years of experience in regulatory medical writing.
• Experience preparing clinical and regulatory submission documents.
• Strong understanding of ICH, CTD, and global regulatory requirements.
• Excellent written and verbal English communication skills.
• Strong analytical thinking and scientific writing ability.
• Good project management and stakeholder management skills.
• Ability to work independently while collaborating with global teams.

Preferred Skills

• Regulatory Medical Writing
• Clinical Trial Documentation
• Clinical Study Reports (CSR/CTR)
• Investigator Brochure (IB)
• CTD Module 2 Writing
• Scientific Communication
• Regulatory Submission Support
• Clinical Development Documentation
• Global Regulatory Compliance
• Medical Writing in Pharmaceutical Industry

Why Join Novo Nordisk?

Employees at Novo Nordisk enjoy:

• Opportunity to work on global clinical development programs.
• International collaboration with experienced medical writing professionals.
• Career growth within a leading multinational pharmaceutical company.
• Continuous learning and professional development.
• Inclusive and innovation-driven work culture.
• Exposure to regulatory submissions across multiple therapeutic areas.
• Competitive salary and employee benefits.

Salary (Estimated)

Based on market benchmarks for Medical Writers with 2–5 years of experience in Bangalore:

₹10,00,000 – ₹16,00,000 per annum (CTC)

Actual compensation will depend on qualifications, skills, and experience.

How to Apply

Application Link