Writer - Gch

3-5 years

Not Disclosed

Bangalore Karnataka

10 Dec. 2, 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

Job Title: Medical Writer – Global Clinical & Health (GCH)
Location: Bangalore, Karnataka, India
Job Type: Full-Time | Regular
Job ID: R-86100

About Lilly

At Lilly, we unite innovation with compassion to improve lives globally. As a leading healthcare company headquartered in Indianapolis, Indiana, Lilly develops life-changing medicines, advances scientific understanding, and supports communities through philanthropy and volunteerism. We prioritize people, innovation, and excellence in everything we do.

We are seeking dedicated professionals committed to improving patient outcomes and advancing medical knowledge. Join us to contribute to impactful medical communications across therapeutic areas.

Position Overview

The Medical Writer – GCH will play a critical role in developing, maintaining, and delivering high-quality scientific and medical content across the drug development lifecycle. This role supports Medical Affairs (MA) initiatives to provide accurate, balanced, and credible medical information to healthcare professionals (HCPs), regulators, payers, and patients.

The writer will contribute to a wide variety of medical content, including:

Slide decks (training, manuscript, EMS, data summaries)
Newsletters and bulletins
QR compendiums and affiliate/regional materials
HCP and patient education materials
Advisory board and competitive landscape presentations
Image sourcing, redraws, and lexicon development
Medical Questions Analysis Documents (MQAD)

This role requires strategic content planning, high-level scientific writing, and collaboration across cross-functional teams to deliver accurate, timely, and compliant medical information.

Key Responsibilities

Content Development & Strategy

Collect, evaluate, and integrate data from multiple sources to develop cohesive medical content strategies.
Plan, draft, edit, and finalize regulatory and MA documents with scientific accuracy and clarity.
Build scientific rationale for complex or strategic documents, ensuring balance and adherence to regulatory and ethical standards.
Coordinate reviews with internal and external experts and incorporate feedback into final deliverables.
Ensure consistency and accuracy across related documents, including data, statements, and conclusions.

Project & Stakeholder Management

Lead writing projects with clear timelines, anticipating risks and mitigating delays.
Communicate project status to stakeholders and escalate issues appropriately.
Collaborate with internal teams and external partners to ensure smooth, timely content delivery.

Knowledge & Skills Development

Maintain therapeutic area expertise, including clinical, pharmacology, and disease-specific knowledge.
Stay current on regulatory and publication guidelines to inform content creation.
Enhance scientific communication skills for varied audiences across digital and print platforms.

Knowledge Sharing & Mentorship

Provide guidance to junior team members and share best practices.
Contribute to process improvements and enhance use of content management systems.

Qualifications & Experience

Required:

Bachelor’s degree in Life Sciences, Health, Communications, or related field.
3–5 years of experience in scientific, regulatory, or medical writing within pharma, biotech, or healthcare.
Proven expertise in developing medical content for HCPs, patients, and regulatory audiences.
Excellent written and verbal English communication skills.
Strong attention to detail, project management, and ability to meet tight deadlines.
Proficiency in MS Office and document management systems.

Preferred:

Graduate degree with research component (MSc, PhD, PharmD).
Experience in clinical development, clinical trial documentation, or regulatory submissions.
Therapeutic area experience in neuroscience, oncology, cardiovascular, immunology, or endocrinology.
Experience in Medical Affairs communications (slide decks, newsletters, patient/HCP materials).
Knowledge of global regulatory guidelines and publication standards.

Why Join Lilly?

Work in a global, innovative healthcare environment with access to cutting-edge medical information projects.
Collaborate with cross-functional experts in Medical Affairs, Regulatory, and Clinical teams.
Opportunity to enhance your scientific communication skills and contribute to patient-centric solutions.
Equal opportunity employer committed to diversity and inclusion.

Experience Level: Mid-level to Senior – 3–5 years of relevant medical/scientific writing experience required.

Apply today to advance your career in medical communications and make a global impact on patient care.

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Writer - Gch

Job Description

About Lilly

Position Overview

Key Responsibilities

Qualifications & Experience

Why Join Lilly?

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