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Medical Writer

Novo Nordisk
2+ years
Not Disclosed
Bangalore, India
1 June 5, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing

Medical Writer

Department: Clinical Development – Clinical Reporting
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Experience Required: Minimum 2+ Years
Industry: Pharmaceutical / Biotechnology / Clinical Research


About the Role

We are seeking a highly motivated and scientifically driven Medical Writer to join the Clinical Reporting team. The successful candidate will be responsible for preparing high-quality regulatory and clinical development documents that support global clinical development programs.

As a Medical Writer, you will collaborate with cross-functional stakeholders across Clinical Development, Medical Affairs, Regulatory Affairs, Biostatistics, Clinical Pharmacology, and Trial Execution teams to ensure accurate, compliant, and impactful communication of clinical trial data and scientific information.

This role requires strong scientific understanding, excellent writing skills, regulatory knowledge, and the ability to translate complex clinical data into clear, concise, and submission-ready documents.


Key Responsibilities

Medical Writing & Clinical Reporting

  • Author, edit, and review clinical and regulatory documents supporting drug development programs.

  • Prepare high-quality clinical reporting documents including:

    • Clinical Trial Protocols

    • Clinical Study Reports (CSRs/CTRs)

    • Investigator’s Brochures (IBs)

    • Clinical Common Technical Document (CTD) Module 2 Summaries and Overviews

    • Regulatory Submission Documents

    • Regulatory Response Documents (Questions & Answers)

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

  • Translate complex scientific and clinical information into clear, concise, and audience-appropriate content.

  • Support both trial and non-trial clinical reporting activities.

Project & Stakeholder Management

  • Serve as a primary contact for stakeholders regarding Clinical Reporting deliverables.

  • Lead discussions and provide recommendations aligned with Clinical Reporting strategies.

  • Collaborate with multidisciplinary teams to define document scope, timelines, and content requirements.

  • Coordinate document development activities to ensure timely delivery of high-quality outputs.

  • Represent the Clinical Reporting function in project teams and cross-functional meetings.

Quality & Compliance

  • Maintain compliance with global regulatory requirements, company standards, and industry guidelines.

  • Apply a quality-focused approach throughout document development and review processes.

  • Ensure documentation is inspection-ready and supports regulatory submissions.

  • Stay updated on evolving regulatory requirements and scientific writing best practices.

Process Improvement & Knowledge Sharing

  • Contribute to continuous improvement initiatives within the Clinical Reporting function.

  • Support implementation of Clinical Reporting strategies and operational excellence initiatives.

  • Mentor junior colleagues and share knowledge within the team.

  • Participate in training programs and capability-building activities.


Required Qualifications

Education

One of the following qualifications is required:

  • PhD in Life Sciences, Pharmacy, Pharmacology, Medicine, Biotechnology, or related discipline

OR

  • Medical Degree (MBBS, MD, or equivalent)

OR

  • Master's Degree such as:

    • MSc

    • M.Pharm

    • Pharm.D

    • Biotechnology

    • Pharmacology

    • Life Sciences

    • Other relevant scientific disciplines

combined with relevant professional experience.


Experience Requirements

Mandatory Experience

  • Minimum 2 years of experience in Regulatory Medical Writing.

  • Experience authoring regulatory and clinical development documents.

  • Understanding of clinical research methodology and drug development processes.

  • Experience working within the pharmaceutical, biotechnology, CRO, or healthcare industry.

Preferred Experience

  • Experience preparing regulatory submission documents for global health authorities.

  • Experience supporting clinical development programs across multiple therapeutic areas.

  • Familiarity with ICH guidelines, GCP principles, and international regulatory requirements.

  • Experience working within global cross-functional teams.