Writer – Global Clinical and Medical Communications (GCH)
Location: Bangalore, Karnataka, India
Category: Medical
Job Type: Full-Time, Regular
Job ID: R-86100
About Lilly
Lilly is a global healthcare leader headquartered in Indianapolis, Indiana, committed to improving lives through scientific discovery and patient-centric innovation. The organization develops life-changing medicines, advances disease understanding, and supports communities through research, philanthropy, and volunteerism. Lilly prioritizes people, scientific excellence, and integrity across its global workforce.
Position Overview
The Writer – GCH role supports the development of high-quality scientific and medical content across the drug development and Medical Affairs lifecycle. This position contributes to clear, accurate, and balanced communication for healthcare professionals, regulators, payers, and patients across global markets.
The Writer will contribute to a wide range of Medical Affairs and scientific communication deliverables, ensuring consistency, compliance, and scientific accuracy.
Key Content Areas Supported
Slide updates and internal training slides
Manuscript and data slide decks
Newsletters and bulletins
QR compendiums
Regional and affiliate slides
Patient and healthcare professional education materials
Advisory board materials
Competitive landscape slides
Image sourcing and redraw
Lexicon development
MQAD (Medical Questions Analysis Document)
Executive Medical Summaries (EMS)
Primary Responsibilities
Content Strategy and Development
Collect and evaluate data from multiple scientific, clinical, and regional sources to plan and execute content strategy.
Organize, author, edit, and finalize scientific and regulatory documents across the clinical development and product lifecycle.
Conduct document initiation meetings to ensure alignment among cross-functional stakeholders.
Develop scientific rationale to support complex and strategic documents.
Ensure clarity, accuracy, and consistency of data interpretation, conclusions, and key messages across connected documents.
Coordinate expert reviews, integrate feedback, and prepare final deliverables.
Ensure all quality checks and compliance steps are completed.
Manage multiple document types across therapeutic areas with flexibility and accuracy.
Collaborate with internal and external experts for preparing scientific presentations.
Support relationship management with vendors or alliance partners as needed.
Project and Stakeholder Management
Lead end-to-end writing processes with strong project management and organizational skills.
Develop and communicate writing timelines; identify and mitigate risks proactively.
Ensure smooth documentation workflows across teams and escalate issues where required.
Provide consistent updates to stakeholders on document status and progress.
Knowledge and Skills Development
Maintain up-to-date knowledge of therapeutic areas, disease states, compounds, and competitive landscapes.
Strengthen understanding of regulatory and publication guidelines.
Demonstrate competency in medical communications tailored to various audiences and platforms.
Contribute to clinical planning, submission strategies, regulatory responses, and scientific literature reviews.
Knowledge Sharing and Collaboration
Share expertise with peers by offering technical guidance and coaching.
Contribute to best practices, process enhancements, and documentation workflows.
Support tool utilization, including document management systems and scientific databases.
Minimum Qualification Requirements
Bachelor’s degree in a scientific, healthcare, communications, or technology-related field.
Demonstrated experience in technical or regulatory scientific writing.
Strong written and verbal communication skills.
Successful completion of a writing assessment as part of the selection process.
Preferred Qualifications
Graduate degree (MSc, MPH, PharmD, PhD) with a research component or specialization in life sciences.
Expertise in therapeutic areas such as neuroscience, oncology, cardiovascular, immunology, or endocrinology.
Experience in:
Regulatory or clinical documentation
Medical Affairs deliverables (slide decks, HCP/patient materials, newsletters)
Clinical development or regulatory processes
Strong project management and time-management capabilities.
Proficiency with scientific writing tools, document systems, word processing, spreadsheets, presentations, and data visualization.
Inclusion and Accessibility
Lilly is committed to providing equal employment opportunities and supporting individuals with disabilities during the application process. Candidates requiring assistance may submit an accommodation request via the official Lilly portal.
Lilly does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity, national origin, disability, veteran status, or any legally protected category.
Gujarat :
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Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Bangor | Brewer |New Jersey :
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Frank Scottile Blvd |Missouri :
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Biberach an der Riß | Freiburg | Grenzach | Heidelberg | Karlsruhe | Konstanz | Stuttgart | Tubingen | Ulm |Hesse :
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Frankfurt | Harveysburg |Germany :
Germany | GErmany |Lower Saxony :
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Ingelheim am Rhein | Mainz |Schleswig Holstein :
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Kyiv |Lima Region :
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Paris | Lyon |South Africa :
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