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Senior Medical Writer

5+ years
Not Disclosed
10 Nov. 6, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Position: Senior Medical Writer
Location: Bangalore, India
Department: Clinical Research
Employment Type: Full-Time
Level: Associate


Job Overview

Seeking a Senior Medical Writer to prepare, review, and manage a variety of clinical and regulatory documents across all clinical trial phases (I–IV) and BA/BE studies. The role ensures high-quality scientific content, regulatory compliance, and smooth cross-functional collaboration.


Key Responsibilities

Clinical & Regulatory Documentation

  • Prepare and review clinical study outlines, feasibility synopses, protocols, and clinical study reports (Phase I–IV, BA/BE).

  • Prepare and review CTD modules for regulatory submissions.

  • Draft and manage Informed Consent Documents (ICDs), Investigator’s Brochures (IBs), subject diaries, and other participant-facing materials.

  • Prepare and review SAE narratives and clinical documents for IND, NDA, BLA, MAA, 505B2, biosimilar, and hybrid applications.

Regulatory Writing & Submission Support

  • Prepare/review Non-Clinical Overview (Module 2.4), Clinical Overview (Module 2.5), and other CTD modules (2.6, 2.7).

  • Develop Integrated Summaries of Safety (ISS) and Efficacy (ISE).

  • Draft briefing packages such as Pre-IND, Pre-NDA, and SAM submissions.

  • Support expedited approval and orphan drug designation processes.

Cross-Functional Collaboration

  • Work with data management, biostatistics, regulatory affairs, and medical teams for document creation and review.

  • Review other study-related documents (SAP, mock TLFs, eCRFs, etc.).

  • Communicate effectively with internal teams, clients, and stakeholders.

Quality & Compliance

  • Ensure compliance with internal SOPs and regulatory writing standards.

  • Prepare/revise departmental SOPs under QA or departmental leadership.

  • Manage administrative and operational tasks within the medical writing department.


Qualifications

Education:
PhD, MBBS, MD, M.Pharm, or Pharm.D in Medical/Pharmacy discipline

Experience:
Minimum 5 years of professional medical writing experience with significant regulatory document contributions.


Skills Required

  • Strong knowledge of clinical and regulatory writing processes.

  • Expert understanding of ICH and regulatory documentation requirements.

  • Proficient in MS Word, PowerPoint, Excel, and Adobe Acrobat (advanced PDF editing preferred).

  • Excellent English communication skills and attention to detail.

  • Ability to multitask, prioritize, and collaborate effectively in cross-functional teams.

Desirable Skills

  • Experience in publication/congress activities and dossier compilation.

  • Strong project ownership and ability to manage writing projects independently.

  • Passion for writing and communicating scientific information.