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Medical Writer

Novo Nordisk
2+ years
INR 8 LPA – 14 LPA
Bangalore, India
1 June 16, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines

Medical Writer

Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Company: Novo Nordisk Global Business Services (GBS)

Position Summary

The Medical Writer is responsible for developing high-quality clinical and regulatory documents that support global clinical development programs. The role involves preparing clinical trial and regulatory submission documents, collaborating with cross-functional stakeholders, ensuring compliance with global regulatory standards, and contributing to the overall Clinical Reporting strategy. The Medical Writer serves as a key scientific communication partner, translating complex clinical data into clear, accurate, and submission-ready documents.

Key Responsibilities

Clinical & Regulatory Medical Writing

  • Prepare, review, and finalize clinical and regulatory documents for global submissions.

  • Develop high-quality scientific content aligned with Clinical Reporting strategies.

  • Ensure consistency, scientific accuracy, and regulatory compliance across all documents.

  • Support clinical development programs through effective scientific communication.

Clinical Trial Documentation

  • Author and review:

    • Clinical Study Protocols

    • Clinical Trial Reports (CTRs/CSRs)

    • Investigator Brochures (IB)

    • Clinical Submission Documents

    • Regulatory Question & Answer (Q&A) Responses

    • CTD Module 2 Summaries and Overviews

  • Ensure documentation complies with ICH and global regulatory requirements.

Stakeholder Management & Collaboration

  • Act as a primary point of contact for Clinical Reporting deliverables.

  • Collaborate with Clinical Development, Medical Affairs, Regulatory Affairs, Biostatistics, and Clinical Operations teams.

  • Facilitate discussions to align document content with project strategies.

  • Coordinate timelines and deliverables with global stakeholders.

Quality & Compliance

  • Apply quality standards throughout document development.

  • Ensure compliance with company SOPs, regulatory requirements, and industry guidelines.

  • Maintain document quality, consistency, and audit readiness.

  • Stay updated on evolving regulatory requirements and best practices.

Project Management

  • Manage multiple writing projects simultaneously.

  • Deliver documents within agreed timelines and quality expectations.

  • Support planning and execution of clinical reporting activities.

  • Identify risks and proactively manage project deliverables.

Knowledge Sharing & Continuous Improvement

  • Mentor junior writers and support capability-building initiatives.

  • Participate in training and knowledge-sharing activities.

  • Contribute to process optimization and operational excellence initiatives.

  • Support innovation and continuous improvement programs.

Educational Qualification

One of the following qualifications:

  • PhD (Life Sciences, Pharmacology, Biotechnology, Biomedical Sciences, or related field)

  • Medical Degree (MBBS / MD)

  • Master's Degree:

    • MSc

    • M.Pharm

    • Pharm.D

    • Equivalent Life Sciences Qualification

Experience Required

  • Minimum 2+ years of Regulatory Medical Writing experience.

  • Experience preparing clinical and regulatory submission documents.

  • Experience in pharmaceutical, biotechnology, CRO, or clinical research industries preferred.

  • Exposure to global regulatory submissions and clinical development programs.

  • Experience working in cross-functional and global environments.