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Senior Medical Writer

GSK plc
8+ years
22 LPA - 40 LPA
Bangalore, India
1 June 22, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: CPT, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, Medical Billing, Medical Coding

Senior Medical Writer

Company: GSK
Location: Bengaluru, India (Hybrid)
Department: Medical Writing / Clinical Regulatory Writing
Employment Type: Full-Time

Role Summary

The Senior Medical Writer is responsible for authoring, reviewing, and managing complex clinical and regulatory documents that support global drug development, regulatory submissions, and clinical research programs. The role involves independently preparing high-quality scientific and regulatory documents, coordinating with cross-functional stakeholders, interpreting clinical trial data, and ensuring compliance with global regulatory standards including ICH-GCP requirements.

Key Responsibilities

Clinical & Regulatory Writing

  • Author and review:

    • Clinical Study Protocols

    • Clinical Study Reports (CSRs)

    • Investigator Brochures (IBs)

    • NDA Submission Documents

    • MAA Submission Documents

    • CTD Modules

    • Regulatory Briefing Documents

    • Responses to Health Authority Queries

  • Ensure scientific accuracy and regulatory compliance across all documents.

Clinical Data Interpretation

  • Interpret and summarize:

    • Clinical Trial Data

    • Efficacy Results

    • Safety Findings

    • Statistical Outputs

  • Ensure accurate representation of study outcomes.

  • Maintain high-quality scientific narratives and conclusions.

Document Development & Management

  • Manage multiple writing projects simultaneously.

  • Drive document planning, drafting, review, approval, and finalization.

  • Coordinate timelines and stakeholder reviews.

  • Ensure consistency across submission packages.

Cross-Functional Collaboration

  • Collaborate with:

    • Clinical Leads

    • Asset Leads

    • Study Delivery Leads (SDLs)

    • Biostatisticians

    • Regulatory Affairs Teams

    • Medical Writers

  • Facilitate effective communication across global teams.

  • Build strong stakeholder partnerships to support document delivery.

Quality & Compliance

  • Ensure compliance with:

    • ICH Guidelines

    • Good Clinical Practice (GCP)

    • Regulatory Submission Standards

    • Company SOPs

  • Maintain document quality, consistency, and data integrity.

  • Participate in planning, review, and quality meetings.

Scientific Communication

  • Support preparation of:

    • Regulatory Submission Packages

    • Clinical Development Documents

    • Scientific Reports

    • Health Authority Communications

  • Promote high medical writing standards across projects.

Required Qualifications

Education

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

  • Master’s Degree with relevant Medical Writing experience

Experience

  • 8+ years of Clinical Regulatory Writing experience in the pharmaceutical industry.

  • Experience authoring:

    • Clinical Study Reports (CSRs)

    • Clinical Trial Protocols

    • Investigator Brochures (IBs)

    • NDA/MAA Submission Documents

    • Regulatory Response Documents