Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.
Post : Medical Writer
Job Description
The Position
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
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.
• 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.
• Share knowledge, mentor colleagues, and contribute to training activities to build capability across the team.
• Apply a quality mindset and maintain up-to-date knowledge of global regulatory requirements and policies relevant to your work.
Candidate Profile
• Must have PhD, Medical degree or Master’s degree (MSc, M Pharm, 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.
Additional Information
Experience : 2+ years
Qualification : PhD, MSc, M Pharm, Pharm.D or equivalent
Location : Bangalore, Karnataka
Industry Type : Pharma / Healthcare / Clinical research
Category : Clinical Reporting
End Date : 20th August 2026
Medical Writer : Apply Online >>
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