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Medical Writer-New-I-Novo-Nordisk

Novo Nordisk
2+ years
INR 6 LPA – 8 LPA
Bangalore, India
1 June 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Medical Writer

Company: Novo Nordisk
Department: Clinical Development – Clinical Reporting
Location: Bangalore, Karnataka, India
Experience: Minimum 2 Years of Regulatory Medical Writing Experience

About the Role

Novo Nordisk is looking for a Medical Writer to join its Clinical Reporting team in Bangalore. The role involves supporting global clinical development programs by preparing high-quality clinical and regulatory documents while ensuring alignment with Clinical Reporting strategies and regulatory requirements.

The selected candidate will serve as a key contact for stakeholders, contribute to strategic discussions, and represent the Clinical Reporting function in cross-functional project teams.

Key Responsibilities

Medical Writing & Clinical Reporting

  • Prepare and author clinical and regulatory documents including:

    • Clinical Trial Protocols

    • Clinical Trial Reports (CTRs)

    • Investigator Brochures (IBs)

    • CTD Module 2 Summaries and Overviews

    • Regulatory Response Documents (Q&A)

  • Deliver high-quality medical writing and clinical reporting outputs within agreed timelines.

  • Ensure documents meet scientific, regulatory, and quality standards.

Project & Stakeholder Management

  • Manage multiple clinical reporting deliverables efficiently.

  • Implement project strategies into clinical and regulatory documents.

  • Engage stakeholders to identify reporting needs, timelines, and deliverable scope.

  • Ensure alignment with Clinical Reporting strategies and project objectives.

Quality & Compliance

  • Maintain a strong quality-focused approach across all deliverables.

  • Stay updated on global regulatory requirements, guidelines, and industry standards.

  • Support process improvement and operational efficiency initiatives.

Knowledge Sharing & Team Development

  • Share expertise and best practices within the team.

  • Support training and mentoring activities.

  • Contribute to capability-building and continuous learning initiatives.

Required Qualifications

Education

  • PhD in Life Sciences, Pharmacy, Medicine, or related field; OR

  • Medical Degree; OR

  • Master's Degree (MSc, M.Pharm, PharmD or equivalent) with relevant experience.

Experience

  • Minimum 2 years of Regulatory Medical Writing experience.

  • Experience across a broad range of scientific and regulatory writing activities.

  • Pharmaceutical industry experience is preferred.

Required Skills

Medical Writing

  • Clinical Trial Protocol Writing

  • Clinical Trial Reports (CTRs)

  • Investigator Brochures (IBs)

  • CTD Module 2 Summaries & Overviews

  • Regulatory Submission Documents

  • Regulatory Response Writing (Q&A)

Scientific & Analytical Skills

  • Strong scientific writing and data interpretation skills.

  • Ability to translate complex scientific information into clear and concise content.

  • Strong analytical and problem-solving abilities.

Project & Stakeholder Management

  • Ability to manage multiple projects and deadlines.

  • Strong stakeholder engagement and communication skills.

  • Experience working with cross-functional global teams.

Communication Skills

  • Excellent written and verbal English communication.

  • Ability to communicate scientific information effectively to diverse audiences.

Additional Attributes

  • High attention to detail and quality mindset.

  • Strong accountability and ownership.

  • Cultural awareness and global collaboration skills.

  • Continuous learning and improvement mindset.