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Medical Writer

Novo Nordisk
2+ years
INR 12 LPA – 20 LPA
Bangalore, India
1 June 10, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines

Medical Writer

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


About the Role

Novo Nordisk is seeking a talented and scientifically driven Medical Writer to join its Clinical Reporting team. This role is responsible for preparing high-quality clinical and regulatory documents that support global clinical development programs.

As a Medical Writer, you will contribute to the development of clinical trial documentation, regulatory submission content, and scientific reports while collaborating with multidisciplinary stakeholders across clinical development, regulatory affairs, biostatistics, and medical functions.

You will serve as a key contributor to clinical reporting activities and ensure that all documents meet regulatory, scientific, and quality standards.


Key Responsibilities

Clinical & Regulatory Medical Writing

  • Prepare, author, and review clinical and regulatory documents.

  • Develop scientifically accurate, clear, and compliant content.

  • Ensure consistency across clinical development documentation.

  • Support global regulatory submissions and clinical reporting activities.

Clinical Trial Documentation

  • Author and maintain:

    • Clinical Trial Protocols

    • Clinical Study Reports (CSRs/CTRs)

    • Investigator Brochures (IBs)

    • Clinical Development Documents

    • Regulatory Response Documents (Q&A)

    • CTD Module 2 Summaries and Overviews

  • Ensure documents align with study objectives and regulatory requirements.

Stakeholder Management

  • Act as the primary contact for Clinical Reporting-related content.

  • Collaborate with cross-functional stakeholders to gather required inputs.

  • Facilitate discussions and drive alignment on document strategy.

  • Represent Clinical Reporting within project teams and working groups.

Project Management & Delivery

  • Manage multiple writing projects simultaneously.

  • Deliver documents within agreed timelines and quality standards.

  • Monitor project milestones and proactively address risks.

  • Support planning and execution of reporting activities.

Document Quality & Compliance

  • Ensure compliance with:

    • ICH Guidelines

    • Regulatory Requirements

    • Internal SOPs

    • Clinical Reporting Standards

  • Perform document reviews and quality checks.

  • Maintain audit-ready documentation practices.

Scientific Communication

  • Translate complex scientific and clinical data into clear, concise, and impactful narratives.

  • Present information tailored to diverse audiences.

  • Ensure accuracy, consistency, and scientific integrity in all deliverables.

Process Improvement & Innovation

  • Support implementation of Clinical Reporting strategies.

  • Participate in process optimization and efficiency initiatives.

  • Contribute to continuous improvement projects.

  • Promote best practices in medical writing and document development.

Knowledge Sharing & Team Development

  • Mentor junior colleagues and support capability-building initiatives.

  • Participate in training activities and knowledge-sharing sessions.

  • Contribute to the development of team expertise and writing standards.


About the Department

The Clinical Reporting Team at Novo Nordisk GBS Bangalore is an integral part of the Global Clinical Reporting organization.

Since its establishment in 2011, the team has grown into a highly specialized group of Medical Writers and Disclosure Medical Writers with expertise across multiple therapeutic areas and regulatory environments.

The department collaborates closely with:

  • Clinical Development

  • Medical & Scientific Affairs

  • Clinical Pharmacology

  • Biostatistics

  • Trial Execution Teams

  • Regulatory Affairs

to ensure high-quality, scientifically robust, and globally compliant clinical documentation.


Required Qualifications

Education

  • PhD in Life Sciences or Related Field

OR

  • M.Pharm

  • Pharm.D

  • M.Sc (Life Sciences)

  • Biotechnology

  • Pharmacology

  • Medicine

  • Equivalent Advanced Scientific Degree


Experience

  • Minimum 2+ years of experience in Regulatory Medical Writing.

  • Experience within the pharmaceutical, biotechnology, CRO, or clinical research industry preferred.

  • Exposure to clinical development and regulatory documentation is highly desirable.