Medical Writer Job at Novo Nordisk, Bangalore
Are you an experienced medical writer looking to contribute to global clinical development and regulatory submissions? Novo Nordisk is inviting applications for the position of Medical Writer at its Global Business Services (GBS) unit in Bengaluru. This Medical Writer Job in Bangalore is ideal for medical and life science professionals with experience in regulatory medical writing and clinical reporting. As a Medical Writer, you will prepare high-quality clinical and regulatory documents while collaborating with global cross-functional teams at Novo Nordisk Careers. If you are passionate about scientific communication and clinical research, this role offers an excellent opportunity to build your career with a globally recognized pharmaceutical company.
About the Company:
Novo Nordisk is a global healthcare company with more than 100 years of experience in discovering and developing innovative treatments for serious chronic diseases. The company is committed to improving the lives of millions of people worldwide through groundbreaking research, scientific excellence, and patient-focused healthcare solutions. Its Global Business Services (GBS) team in India plays a vital role in supporting clinical development, regulatory submissions, and global healthcare initiatives.
Job Details:
- Job Title: Medical Writer
- Department: Clinical Reporting
- Business Unit: Global Business Services (GBS)
- Job Location: Bengaluru, Karnataka, India
- Employment Type: Full-Time
- Category: Clinical Development
- Application Deadline: 20th July 2026
Your New Role:
As a Medical Writer, you will perform a wide range of medical writing tasks to support clinical development programs, delivering high-quality content and documents that align with the Clinical Reporting strategy. The tasks for trial and/or non-trial activities within clinical reporting will include but will not be limited to preparation of Protocols, Clinical Trial Reports (CTRs), Investigator Brochure (IB), CTD Module 2 summaries and overview (clinical submission documents) and Regulatory response documents (Q&A).
You will act as a primary contact for stakeholders on Clinical Reporting-driven content, drive discussions to ensure decisions align with strategy, and represent Clinical Reporting in relevant project groups.
Your New Department:
The Clinical Reporting unit in GBS has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community, since its inception in 2011. The team is a dynamic mix of enthusiastic and qualified skilled Medical Writer and, Disclosure Medical Writers with Masters/PhD in life sciences, pharmacology, medicine, etc. The team is full of commitment, passion, skills, and talent with broad knowledge on different therapeutic areas and regulatory requirements for submissions. The team has an average experience of 7 to 8 years in writing and reviewing regulatory documents. We use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials. The department partners closely with cross-functional stakeholders across Medical and Science, Clinical Pharmacology, Biostatistics, Trial Execution, and Regulatory Affairs. The department emphasizes knowledge sharing, innovation, and continuous improvement to support multi-regional clinical studies and ensure cohesive, high-quality deliverables.
Key Responsibilities:
- Efficiently manage and deliver on clinical reporting and medical writing deliverables while maintaining high quality standards.
- Implement project strategies into documents and review project/study-specific materials as needed in this Non-Clinical Job.
- Engage stakeholders to identify needs, timing and scope of clinical reporting deliverables and ensure alignment with the Clinical Reporting strategy.
- Support execution of the Clinical Reporting vision and contribute to process improvements and efficiency initiatives in this Medical Writer Job in Bangalore.
- Share knowledge, mentor colleagues, and contribute to training activities to build capability across the team at Novo Nordisk Careers.
- Apply a quality mindset and maintain up-to-date knowledge of global regulatory requirements and policies relevant to your work.
Your Skills and Qualifications for the Medical Writer Job:
To be successful in this role, you should have the following qualifications:
- Must have PhD, Medical degree or Master’s degree (Pharm D or equivalent) combined with relevant experience.
- Experience: At least 2 years’ experience in regulatory medical writing
- Experience across a broad range of scientific writing tasks; experience in the pharmaceutical industry or equivalent is desirable
- Able to work independently on well-defined tasks with appropriate guidance, strong analytical skills, persistence, accountability, and ability to manage variable workloads.
- Communication: Fluent in written and spoken English with the ability to translate complex scientific data into clear, concise, and engaging content tailored to diverse audiences.
- Collaboration & stakeholder management: Good project management skills; skilled at fostering cross-functional collaboration across multidisciplinary teams and maintaining professional, trustworthy communication with integrity.
- Additional attributes: Cultural awareness for global collaboration, willingness to seek feedback and continuously improve, and a quality-focused mindset.
