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Senior Medical Reviewer Gch

Lilly
2+ years
INR 18 LPA – 35 LPA
Bangalore, India
1 July 2, 2026
Job Description
Job Type: Full Time Education: MBBS/MD/ BAMS/ BDS/ MDS Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Senior Medical Reviewer – Global Content Hub (GCH)

Company: Eli Lilly
Location: Bengaluru, India
Department: Global Content Hub (GCH) / Medical Affairs / Commercial Medical
Job Type: Full-Time
Experience: 2+ Years


JOB OVERVIEW

The Senior Medical Reviewer – Global Content Hub (GCH) is responsible for providing scientific and medical review of promotional and non-promotional materials to ensure medical accuracy, regulatory compliance, and scientific integrity. The role collaborates with Commercial, Medical Affairs, Clinical Research, Marketing, Regulatory, Legal, and Compliance teams to develop, review, and approve medical content, support scientific communications, contribute to brand strategy, and deliver high-quality medical information for healthcare professionals and internal stakeholders.


KEY RESPONSIBILITIES

Medical Review & Scientific Quality

  • Review promotional materials.

  • Review non-promotional medical content.

  • Ensure scientific accuracy.

  • Verify medical claims.

  • Ensure regulatory compliance.

  • Perform medical quality review.

  • Support medical content approval.

  • Maintain scientific consistency.

  • Ensure content aligns with company standards.

Medical Affairs Support

  • Support Medical Affairs teams.

  • Collaborate with Commercial teams.

  • Serve as medical subject matter expert.

  • Provide therapeutic area expertise.

  • Support brand medical strategies.

  • Contribute to local brand plans.

  • Support medical communication initiatives.

Scientific Content Development

  • Review scientific presentations.

  • Support slide deck development.

  • Review medical publications.

  • Contribute to abstracts.

  • Review scientific posters.

  • Support manuscript development.

  • Develop scientific communication materials.

  • Review global and regional medical content.

Scientific Literature & Evidence Review

  • Critically evaluate medical literature.

  • Review published clinical evidence.

  • Monitor therapeutic advancements.

  • Stay current with treatment guidelines.

  • Assess clinical practice trends.

  • Support Scientific Data Disclosure (SDD) plans.

  • Interpret clinical research findings.

Cross-Functional Collaboration

  • Partner with Clinical Research Physicians (CRPs).

  • Collaborate with Clinical Research Scientists (CRSs).

  • Support Medical Science Liaisons (MSLs).

  • Work with Marketing teams.

  • Collaborate with Regulatory Affairs.

  • Coordinate with Compliance teams.

  • Partner with Legal teams.

  • Support payer-related medical initiatives.

Medical Training

  • Support internal medical training.

  • Deliver scientific education.

  • Provide therapeutic area guidance.

  • Train internal stakeholders.

  • Share medical knowledge with business partners.

Scientific Data Analysis

  • Analyze clinical data.

  • Interpret study outcomes.

  • Support publication development.

  • Review scientific evidence.

  • Translate clinical data into meaningful medical content.

  • Provide evidence-based recommendations.

Regulatory & Compliance

  • Ensure compliance with medical regulations.

  • Follow internal SOPs.

  • Maintain ethical medical communication.

  • Support medical governance.

  • Ensure regulatory-ready content.

Stakeholder Engagement

  • Communicate with cross-functional teams.

  • Participate in medical discussions.

  • Influence scientific decision-making.

  • Support customer-focused medical initiatives.

  • Collaborate across global teams.

Continuous Learning

  • Stay updated with therapeutic advances.

  • Monitor clinical practice developments.

  • Follow emerging scientific evidence.

  • Maintain expertise in assigned therapy areas.

  • Support continuous improvement initiatives.


EDUCATIONAL QUALIFICATIONS

Required

  • MBBS

  • BDS

  • PharmD

  • MSc Nursing

  • Master's Degree in Health Sciences

  • Bachelor's Degree in Health Sciences

Preferred

  • MD

  • PhD

  • Advanced Clinical Degree


EXPERIENCE REQUIREMENTS

Required

  • Minimum 2 years of clinical or therapeutic experience.

  • Relevant pharmaceutical or biotechnology industry experience.

  • Experience in Medical Affairs or Scientific Review.

Preferred

  • Experience reviewing promotional and non-promotional materials.

  • Experience supporting scientific publications.

  • Experience in therapeutic area medical strategy.