NovoNordisk is hiring Pharm D & MPharm Graduates | Medical Writer Job | Apply Now
Looking for an exciting Medical Writer Job in Clinical Development? This Pharma Job at Novo Nordisk Global Business Services in Bangalore offers an opportunity to shape clinical reporting and regulatory submissions across global programs. Join a dynamic team, collaborate with key stakeholders, and grow your career in a challenging and rewarding environment.
- Job Title: Medical Writer – Clinical Development
- Location: Bangalore, Karnataka, IN
About the Company
Novo Nordisk Global Business Services (GBS), India, is a leading global pharmaceutical company with over 100 years of experience in defeating chronic diseases. GBS India provides top-tier support for clinical reporting, regulatory submissions, and multi-regional studies, ensuring impactful communication of clinical trial outcomes. Working here gives you exposure to innovative practices and career growth in the pharma industry.
Job Description
- Perform medical writing tasks to support clinical development programs (Medical Writer Job).
- Prepare Protocols, Clinical Trial Reports (CTRs), Investigator Brochures, and CTD Module 2 documents.
- Develop regulatory response documents and submission content.
- Ensure all deliverables align with the Clinical Reporting strategy.
- Act as a primary contact for stakeholders and drive strategic alignment.
- Contribute to clinical reporting and regulatory submissions in a global Pharma Job environment.
Key responsibilities
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- Manage and deliver medical writing and clinical reporting work with high quality.
- Follow project plans and review study-related documents.
- Work with stakeholders to understand requirements and timelines.
- Support team goals and help improve processes.
- Share knowledge, guide team members, and help with training.
- Stay updated with global regulatory guidelines and maintain quality standards.
Qualifications
- Master’s, PhD, or Medical degree (MSc, M Pharm, Pharm D, or equivalent) with relevant experience.
- At least 2 years of experience in regulatory medical writing.
- Experience in scientific writing; pharma industry experience is a plus.
- Ability to work independently with strong analytical and problem-solving skills.
- Good communication skills in English, with the ability to explain complex data clearly.
- Strong teamwork and stakeholder management skills.
- Good project management and ability to work with different teams.
- Willingness to learn, improve, and maintain a high-quality work approach.
Last Date to Apply
- 8th April 2026
