Medical Writer Job in Bangalore at Novo Nordisk. Apply for clinical development writing role with regulatory experience before April 8 deadline.
Introduction
Medical writing is one of the most specialized and rewarding career paths in clinical research and pharmaceutical development. If you have experience in regulatory writing and enjoy transforming scientific data into clear, structured documents, this opportunity can elevate your career. A global healthcare leader is hiring Medical Writers in Bangalore to support clinical development and regulatory submissions.
Company Overview
Novo Nordisk is a globally renowned pharmaceutical company with over a century of experience in developing innovative treatments for chronic diseases. The organization is known for its strong focus on research, patient-centric healthcare solutions, and global clinical development programs. Its Global Business Services (GBS) division in India plays a key role in supporting international operations, including clinical reporting and regulatory documentation.
Job Overview
| Job Details | Information |
|---|---|
| Job Role | Medical Writer – Clinical Development |
| Company | Novo Nordisk |
| Location | Bangalore, Karnataka |
| Experience | Minimum 2 Years |
| Qualification | MSc / M.Pharm / Pharm.D / PhD / Medical Degree |
| Employment Type | Full-Time |
| Department | Clinical Reporting |
| Application Mode | Online |
| Last Date | April 8, 2026 |
Job Location & Employment Type
- Location: Bangalore, Karnataka
- Employment Type: Full-time
- Department: Clinical Reporting (GBS India)
Open Positions / Department Details
- Department: Clinical Reporting
- Role Level: Mid-level (Experienced professionals)
- Work Area: Regulatory Medical Writing & Clinical Documentation
- Team: Global clinical reporting team collaborating with cross-functional stakeholders
Key Roles & Responsibilities
As a Medical Writer, you will be responsible for developing high-quality clinical and regulatory documents. Your responsibilities include:
- Preparing clinical documents such as Protocols, Clinical Study Reports (CSRs), and Investigator Brochures
- Writing CTD Module 2 summaries and clinical overviews for regulatory submissions
- Supporting regulatory responses and Q&A documentation
- Collaborating with stakeholders across clinical, regulatory, and scientific teams
- Ensuring alignment with clinical reporting strategies and project goals
- Reviewing and editing scientific content for accuracy and clarity
- Managing multiple writing projects while maintaining timelines and quality
- Contributing to process improvements and efficiency initiatives
- Mentoring junior team members and supporting training activities
- Staying updated with global regulatory guidelines and writing standards
Eligibility Criteria
Education
Candidates must have one of the following:
- MSc (Life Sciences / Pharmacology / Related field)
- M.Pharm
- Pharm.D
- PhD or Medical Degree
Experience
- Minimum 2 years of experience in regulatory medical writing
- Experience in pharmaceutical industry or CRO preferred
- Exposure to multiple types of clinical/regulatory documents
Skills Required
Candidates should demonstrate:
- Strong scientific writing and analytical skills
- Ability to convert complex clinical data into clear, concise content
- Excellent written and spoken English communication
- Knowledge of global regulatory guidelines (ICH, CTD, etc.)
- Project management and stakeholder coordination skills
- Ability to work independently and manage multiple deadlines
- Attention to detail and quality-focused mindset
- Collaboration skills for cross-functional teamwork
Salary & Benefits
- Salary: As per company norms
- Opportunity to work in a global pharmaceutical company
- Exposure to international clinical development programs
- Learning and career growth opportunities
- Collaborative and innovation-driven work environment
- Professional development and training programs
Selection Process
The selection process may include:
- Resume shortlisting
- Technical/medical writing assessment
- Interview rounds (technical + stakeholder discussion)
- HR discussion and final offer
How to Apply
Interested candidates must apply through the official company careers portal.
- Upload your updated CV online
- No separate cover letter required
- Include a short motivation statement in your CV
Important Dates
- Last Date to Apply: April 8, 2026
- Early application is recommended
Why Apply for This Pharma Job?
This role offers a strong platform for professionals looking to grow in regulatory medical writing. By applying, you can:
- Work on global clinical trial documentation
- Gain expertise in regulatory submissions and CTD writing
- Collaborate with international scientific and clinical teams
- Build a long-term career in medical writing and clinical development
- Be part of a globally respected pharmaceutical organization
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with Novo Nordisk or its hiring team. We do not charge any fees or participate in recruitment. Candidates are advised to verify details and apply through official channels only.
Final Call-to-Action
If you have experience in medical writing and want to work on global clinical development projects, this is an excellent opportunity. Apply now before the deadline and advance your career in regulatory medical writing.
