Novo Nordisk Hiring Medical Writers Bangalore | Apply Now
Novo Nordisk Hiring Medical Writers in Bangalore | M.Pharm, Pharm.D, MSc Candidates Apply
Professionals with experience in regulatory medical writing have an excellent opportunity to join Novo Nordisk, one of the world’s leading healthcare and biopharmaceutical companies. The company is currently hiring for the position of Medical Writer in Bangalore within its Clinical Development division. This role offers the chance to contribute to global clinical development programs while working on regulatory and scientific documents that support drug development and regulatory submissions across international markets.
Medical writing has become one of the most sought-after career paths in the pharmaceutical industry, particularly for candidates with backgrounds in pharmacy, life sciences, medicine, and clinical research. With increasing regulatory requirements worldwide, skilled medical writers play a critical role in preparing clinical trial documents, regulatory submissions, clinical study reports, investigator brochures, and scientific communications.
For candidates seeking pharmaceutical jobs in Bangalore, regulatory affairs careers, clinical development opportunities, or medical writing jobs in India, this opening at Novo Nordisk presents a valuable career advancement opportunity.
Company Overview
Novo Nordisk is a globally recognized healthcare company with more than 100 years of experience in developing treatments for chronic diseases. The organization focuses on improving patient outcomes through scientific innovation, research excellence, and healthcare advancements.
The company’s Global Business Services (GBS) center in Bangalore serves as a strategic hub supporting worldwide operations across clinical development, regulatory affairs, medical affairs, pharmacovigilance, and scientific communication functions.
The Clinical Reporting department at Novo Nordisk is an integral part of the global clinical development ecosystem. The team consists of highly experienced medical writers, disclosure specialists, scientists, pharmacists, and healthcare professionals who contribute to the preparation of regulatory documents supporting clinical trials and product registrations worldwide.
Job Role & Responsibilities
Position: Medical Writer
As a Medical Writer, you will support clinical development programs by preparing high-quality scientific and regulatory documents required for global drug development activities. The role involves collaboration with cross-functional stakeholders including clinical scientists, biostatisticians, regulatory affairs specialists, clinical pharmacologists, and medical experts.
Key Responsibilities
Clinical and Regulatory Document Preparation
- Prepare clinical study protocols.
- Develop Clinical Trial Reports (CTRs).
- Create Investigator Brochures (IBs).
- Prepare CTD Module 2 summaries and overviews.
- Draft regulatory response documents and query responses.
- Develop scientific content supporting regulatory submissions.
Clinical Reporting Activities
- Deliver medical writing projects within defined timelines.
- Ensure document quality, consistency, and compliance.
- Translate clinical data into scientifically accurate narratives.
- Review study-specific materials and clinical documentation.
- Support global submission activities.
Stakeholder Management
- Act as a primary point of contact for clinical reporting activities.
- Collaborate with global clinical development teams.
- Facilitate discussions related to document strategy.
- Represent Clinical Reporting functions in project meetings.
- Ensure alignment with overall clinical reporting objectives.
Process Improvement and Knowledge Sharing
- Support continuous improvement initiatives.
- Contribute to standardization of medical writing processes.
- Mentor junior colleagues and support training activities.
- Share scientific and regulatory knowledge within the team.
- Promote quality-focused documentation practices.
Regulatory Compliance
- Maintain awareness of global regulatory requirements.
- Follow applicable guidelines for clinical reporting.
- Ensure compliance with international submission standards.
- Support preparation of regulatory documentation packages.
Eligibility / Qualifications
Educational Qualification
Candidates must possess one of the following qualifications:
- PhD in Life Sciences or related discipline
- Medical Degree
- M.Pharm
- Pharm.D
- MSc
- Equivalent postgraduate qualification in life sciences
Relevant Courses
M.Pharm, Pharm.D, MSc Pharmacology, MSc Clinical Research, MSc Biotechnology, MSc Life Sciences, MSc Biochemistry, MSc Microbiology, MSc Molecular Biology, Pharmaceutical Sciences, Medical Sciences, Clinical Pharmacology, Drug Regulatory Affairs, Biomedical Sciences, Toxicology, PhD Life Sciences, PhD Pharmacology, MBBS, MD.
Experience Required
- Minimum 2 years of experience in Regulatory Medical Writing.
- Experience within pharmaceutical, biotechnology, CRO, or healthcare sectors is preferred.
- Exposure to clinical development documentation is advantageous.
Essential Skills
- Regulatory Medical Writing
- Clinical Trial Documentation
- Clinical Study Reports (CSR/CTR)
- Investigator Brochure Preparation
- Protocol Writing
- Regulatory Submission Support
- Scientific Writing
- Clinical Research Knowledge
- Regulatory Affairs Understanding
- Data Interpretation Skills
- Project Management
- Stakeholder Communication
- Scientific Literature Analysis
- Technical Writing
Why Consider a Career in Medical Writing?
Medical writing remains one of the fastest-growing specialized functions within pharmaceutical research and development. Regulatory agencies worldwide require comprehensive scientific documentation to support clinical trials, product approvals, lifecycle management, and post-marketing activities.
Career Growth Opportunities
Medical Writers can progress into roles such as:
- Senior Medical Writer
- Principal Medical Writer
- Regulatory Writing Specialist
- Clinical Documentation Lead
- Scientific Communications Manager
- Clinical Reporting Manager
- Regulatory Affairs Manager
- Medical Affairs Specialist
The role also provides significant exposure to clinical development, regulatory strategy, healthcare analytics, and pharmaceutical product development.
Working Environment at Novo Nordisk
The Clinical Reporting team in Bangalore collaborates closely with global stakeholders across multiple therapeutic areas and clinical development programs. Team members gain exposure to:
- International regulatory submissions
- Global clinical trials
- Scientific communication projects
- Cross-functional pharmaceutical operations
- Multi-regional development programs
- Advanced clinical reporting technologies
The organization promotes knowledge sharing, innovation, continuous learning, and professional development while maintaining high scientific and regulatory standards.
Location & Salary
Location: Bangalore, Karnataka
Salary: ₹12 LPA – ₹22 LPA (Approximate market range based on experience, medical writing expertise, and pharmaceutical industry standards)
Application Process
Interested candidates can apply through the official Novo Nordisk careers portal.
Apply Online: https://careers.novonordisk.com/job/Bangalore-Medical-Writer-Karn/1400402533/
Application Deadline
Last Date to Apply: 19 June 2026
Important Note
Applicants are not required to submit a separate cover letter. However, Novo Nordisk recommends including a brief statement about your motivation and career interests within your CV or resume.
Frequently Asked Questions (FAQs)
1. What qualifications are required for the Novo Nordisk Medical Writer role?
Candidates should hold a PhD, Medical Degree, M.Pharm, Pharm.D, MSc, or an equivalent life sciences qualification.
2. Is prior medical writing experience mandatory?
Yes. A minimum of 2 years of regulatory medical writing experience is required.
3. Where is the job located?
The position is based in Bangalore, Karnataka.
4. What documents will Medical Writers prepare?
The role includes preparation of Protocols, Clinical Trial Reports, Investigator Brochures, CTD summaries, and regulatory response documents.
5. What is the expected salary range?
The approximate salary range is ₹12–22 LPA depending on qualifications and experience.
6. What is the last date to apply?
Applications are open until 19 June 2026.
Summary Table
| Company | Novo Nordisk |
|---|---|
| Department Vacancies | Clinical Development – Medical Writer |
| Qualification | PhD, Medical Degree, M.Pharm, Pharm.D, MSc, Life Sciences |
| Experience | Minimum 2 Years |
| Location | Bangalore |
