Medical Writer Job at Novo Nordisk, Bangalore
Want to use your scientific expertise to shape global clinical research and drug development? Novo Nordisk is hiring a Medical Writer for its Clinical Reporting team in Bangalore. This Medical Writer Job in Bangalore is an excellent opportunity for professionals with experience in regulatory medical writing and clinical development. The role involves creating high-quality clinical and regulatory documents that support global drug development programs. Candidates at Novo Nordisk Careers will work closely with multidisciplinary teams and contribute to impactful healthcare innovations. If you have a strong scientific background and a passion for communicating complex clinical data, this position could be an ideal fit.
About the Company:
Novo Nordisk is a globally recognized healthcare company with a history spanning more than 100 years. The organization is dedicated to defeating serious chronic diseases and improving the lives of millions of people worldwide through innovative healthcare solutions.
With a strong presence across global markets, Novo Nordisk focuses on developing treatments for chronic diseases while continuously advancing scientific research and healthcare innovation. The company fosters a culture of collaboration, curiosity, inclusion, and professional growth, empowering employees to make a meaningful impact on global health.
The Clinical Reporting unit within Novo Nordisk Global Business Services (GBS) has become an integral part of the Global Clinical Reporting community since its establishment in 2011. The department consists of highly qualified Medical Writers and Disclosure Medical Writers with expertise across multiple therapeutic areas and regulatory requirements, supporting clinical studies and regulatory submissions worldwide.
Job Details:
- Job Title: Medical Writer
- Department: Clinical Development – Clinical Reporting
- Location: Bangalore, Karnataka, India
- Employment Type: Full-Time
- Work Mode: On-Site
- Industry: Pharmaceutical and Healthcare
- Application Mode: Online
- Application Deadline: 19 June 2026
- Team: Clinical Reporting
- Experience Required: Minimum 2 Years in Regulatory Medical Writing
Key Responsibilities:
- Prepare high-quality clinical and regulatory documents for clinical development programs.
- Develop Protocols, Clinical Trial Reports (CTRs), Investigator Brochures (IBs), and CTD Module 2 summaries and overviews in this Medical Writer Job in Bangalore
- Create Regulatory Response documents and Question & Answer submissions.
- Serve as the primary point of contact for stakeholders on Clinical Reporting content.
- Drive discussions and ensure alignment with Clinical Reporting strategies.
- Implement project strategies into scientific and regulatory documents at Novo Nordisk Careers
- Review project-specific and study-specific materials.
- Coordinate with stakeholders to define timelines, scope, and deliverables.
- Contribute to process improvement and operational efficiency initiatives.
- Mentor colleagues and participate in training and knowledge-sharing activities in this Job in Bangalore
- Maintain compliance with global regulatory requirements and company policies.
- Represent Clinical Reporting in cross-functional project teams.
Educational Requirements for this Medical Writer Job:
- PhD in a relevant scientific discipline OR
- Medical Degree from a recognized institution OR
- Master’s Degree, such as Pharm.D
- Relevant experience in regulatory medical writing is mandatory.
Skills Required:
- Regulatory Medical Writing expertise.
- Clinical Trial documentation experience.
- Scientific and technical writing proficiency.
- Strong understanding of clinical development processes.
- Knowledge of global regulatory requirements.
- Excellent analytical and problem-solving skills.
- Ability to translate complex scientific information into clear content.
- Strong project management capabilities.
- Stakeholder management and collaboration skills.
- Excellent written and verbal English communication skills.
- Ability to work independently and manage multiple priorities.
- Quality-focused mindset and attention to detail.
- Cross-functional teamwork and leadership abilities.
- Adaptability in a global and multicultural work environment.
Benefits of the Medical Writer Job:
- Opportunity to work with one of the world’s leading pharmaceutical companies.
- Exposure to global clinical development and regulatory submission projects.
- Collaboration with experienced scientific and medical professionals.
- Continuous learning and professional development opportunities.
- Participation in innovative healthcare and drug development initiatives.
- Access to a highly skilled and knowledge-driven work environment.
- Opportunities for career growth within a global organization.
- Inclusive and diverse workplace culture.
- Exposure to multiple therapeutic areas and international regulatory frameworks.
- Chance to contribute to life-changing healthcare solutions impacting millions of patients worldwide.
