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Senior Medical Writer 443281

GSK plc
8+ years
INR 28 LPA – 45 LPA
Bangalore, India
1 June 23, 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

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

Role Summary

The Senior Medical Writer is responsible for independently authoring, reviewing, and coordinating complex clinical and regulatory documents that support drug development, regulatory submissions, and clinical research programs. The role requires strong expertise in clinical trial design, statistical data interpretation, regulatory writing, and stakeholder management to ensure delivery of high-quality, scientifically accurate, and regulatory-compliant documentation.

The position works closely with Clinical Leads, Asset Leads, Biostatisticians, Study Delivery Leads, and cross-functional global teams to support product development and regulatory submissions.

Key Responsibilities

Clinical & Regulatory Writing

  • Author and review:

    • Clinical Study Protocols

    • Clinical Study Reports (CSRs)

    • NDA Submission Documents

    • MAA Submission Documents

    • CTD Modules

    • Investigator Brochures (IBs)

    • Briefing Documents

    • Regulatory Response Documents

  • Ensure compliance with global regulatory requirements and company standards.

  • Deliver high-quality scientific and regulatory documentation.

Data Interpretation & Scientific Communication

  • Interpret:

    • Clinical Trial Data

    • Statistical Analysis Results

    • Efficacy Data

    • Safety Data

  • Ensure scientific accuracy and consistency across all documents.

  • Translate complex clinical data into clear regulatory narratives.

Document Development & Coordination

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

  • Coordinate with document teams and stakeholders.

  • Manage multiple writing projects simultaneously.

  • Ensure timely delivery of assigned documents.

Quality & Compliance

  • Maintain consistency, accuracy, and quality of deliverables.

  • Ensure compliance with:

    • ICH Guidelines

    • GCP Standards

    • Regulatory Submission Requirements

    • Internal SOPs

  • Perform document reviews and quality checks.

Stakeholder Management

  • Collaborate with:

    • Clinical Leads

    • Asset Leads

    • Study Delivery Leads (SDLs)

    • Biostatisticians

    • Regulatory Teams

    • Medical Writers

  • Facilitate communication across global cross-functional teams.

  • Build strong working relationships to support document development.

Process Improvement & Leadership

  • Identify issues and propose improvements proactively.

  • Promote best practices in medical writing.

  • Support development of high-quality writing standards.

  • Participate in planning, review, and coordination meetings.

Required Qualifications

Education

One of the following:

  • PhD in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Pharmacology

    • Medical Sciences

    • Related Scientific 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)

    • Protocols

    • NDA/MAA Submissions

    • CTD Documents

    • Investigator Brochures

    • Regulatory Response Documents

  • Experience working with global cross-functional teams.