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Senior Medical Information Writer

2-5 years
Not Disclosed
10 Nov. 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Senior Medical Information Writer

Location: Hyderabad, India
Job Type: Full-Time
Category: Medical Information / Medical Writing

Role Overview

The Senior Medical Information Writer is responsible for developing high-quality, evidence-based scientific content to support global and local medical information needs. This role requires strong expertise in literature evaluation, medical writing, and the creation of scientifically accurate and compliant response documents across therapeutic areas. The position directly contributes to advancing medical communication excellence and ensuring timely, accurate scientific support for healthcare stakeholders worldwide.

Key Responsibilities

Scientific Content Development

  • Conduct comprehensive literature searches, assess scientific publications, and extract relevant clinical and scientific data.

  • Develop accurate, fair-balanced, evidence-based summaries for scientific response documents across assigned therapeutic areas.

  • Adapt global scientific response documents to country-specific requirements.

  • Prepare responses to escalated medical information inquiries.

  • Contribute to US NDA Annual Reports and US compendia reviews.

  • Peer-review content produced by other writers to ensure quality, accuracy, and consistency.

Medical Information Operations

  • Maintain deep therapeutic area knowledge to support content development.

  • Collaborate with Global Medical Information (GMI) teams to implement content plans and deliver assigned scientific materials.

  • Ensure timely delivery of scientific response documents, annual reports, and compendia reviews according to established timelines.

  • Participate in cross-functional project teams and ensure completion of assigned tasks.

Stakeholder Collaboration

  • Build strong working relationships with medical and scientific stakeholders across the global business units.

  • Engage effectively with Medical Affairs, Pharmacovigilance, and other internal teams to gather information and align on scientific content.

  • Support knowledge sharing by mentoring and guiding junior medical information writers.

Process Excellence & Compliance

  • Act as a subject matter expert in medical information writing and maintain awareness of relevant regulatory standards for supported markets.

  • Support medical information teams in assessing annual content needs and implementing content strategies.

  • Partner with approved vendors to ensure compliant and high-quality deliverables.

  • Use stakeholder feedback to refine content quality, scientific accuracy, and training materials.

Required Experience and Qualifications

  • More than 5 years of experience in medical writing within the pharmaceutical or healthcare industry, or equivalent experience in a clinical environment.

  • At least 2–3 years of direct medical information experience in a pharmaceutical company.

  • Excellent scientific writing and editing skills with proven expertise in literature evaluation, data interpretation, and multi-level response development.

  • Advanced degree in Life Sciences, Pharmacy, Medicine, or related field (PharmD, PhD, MSc, MBA, or equivalent).

  • Strong communication skills, ability to collaborate across teams, and capability to work independently.

  • Excellent proficiency in written and spoken English.

  • Experience managing deadlines, delivering high-quality content, and operating within global scientific processes.

Soft Skills

  • Strong stakeholder management and interpersonal communication.

  • Ability to work in a global, matrixed environment.

  • Attention to detail, time management, and scientific accuracy.

  • High level of accountability, organization, and adaptability.

Why Join

This role offers the opportunity to contribute to scientifically meaningful work across a diverse portfolio, ranging from established medicines to transformative innovations in chronic disease and immunology. You will work with advanced digital tools, AI-enabled systems, and global experts who are redefining the future of medical information and scientific communication.

Equal Opportunity Statement

The organization is committed to fostering an inclusive and diverse workplace. All qualified applicants are considered without regard to race, color, ancestry, religion, sex, national origin, sexual orientation, gender identity, age, marital status, disability, citizenship, veteran status, or any other protected characteristics.