Medical Writing - Medical Affairs
English
₹15000/MONTH
1 Year
Bachelor's degree
Work From Office
Date Posted
07-Jul-2026
Location
Karnataka (KA), 1
Job Type
Full Time
Company
Huntsman
Description
Job Details
???? Job Title: Medical Writer – Medical Affairs
???? Location: Bengaluru, Karnataka
???? Job Type: Full-time
About Lilly
At Lilly, we unite caring with discovery to improve lives worldwide. As a global healthcare leader headquartered in Indianapolis, Indiana, our mission is to discover and deliver life-changing medicines while advancing the understanding and management of diseases. Our employees are dedicated to innovation, scientific excellence, and patient-centered care.
Position Overview – Medical Writing (Medical Affairs)
Medical Affairs (MA) at Lilly plays a crucial role in providing clear, credible, and evidence-based answers to regulators, healthcare providers, payers, and patients. Our team focuses on developing high-quality scientific content to support Medical Affairs activities across the drug development lifecycle.
Scope of Work – Key Content Development Areas
The Medical Affairs content development team is responsible for creating and maintaining various types of medical and scientific materials, including:
✅ Scientific Slide Decks: Manuscript slides, data slides, internal training slides, advisory board slides, competitive landscape slides.
✅ Publications & Reports: Newsletters, bulletins, executive medical summaries (EMS).
✅ Educational Materials: HCP and patient education materials, lexicon, medical question analysis documents (MQAD).
✅ Visual & Design Work: Image sourcing, image redraws, QR compendium.
Primary Responsibilities
1️⃣ Content Strategy & Execution
- Plan, write, edit, and finalize regulatory and medical documents in alignment with scientific standards.
- Conduct document initiation meetings to ensure clarity and alignment among stakeholders.
- Present data in a clear, accurate, concise, and balanced manner.
- Ensure consistency of key statements and conclusions across related documents.
- Coordinate scientific reviews and integrate feedback for finalization.
- Maintain quality control and conduct accuracy checks.
2️⃣ Project & Stakeholder Management
- Lead the writing process with effective project management to meet timelines.
- Build and communicate credible project timelines with internal teams.
- Anticipate risks and roadblocks in content development and mitigate them proactively.
- Collaborate with internal and external experts for scientific presentations.
- Work with vendors and alliance partners, if necessary.
3️⃣ Knowledge Development & Scientific Expertise
- Stay updated on therapeutic area knowledge (e.g., neuroscience, oncology, cardiovascular, immunology, endocrinology).
- Adapt to different document types, therapeutic areas, and drug development phases.
- Maintain knowledge of regulatory guidelines and scientific communication standards.
- Analyze competitor landscape and contribute insights to clinical planning.
4️⃣ Knowledge Sharing & Process Improvement
- Mentor and guide peers by sharing expertise in scientific communication.
- Identify and share best practices across functions and regions.
- Contribute to process improvements for better content development workflows.
- Provide expertise in document management systems and related tools.
Qualifications & Requirements
✅ Minimum Qualifications
???? Education:
- Bachelor’s degree in a scientific, healthcare, communications, or technology-related field.
✍️ Writing & Communication Skills:
- Experience in technical/regulatory scientific writing.
- Strong written and verbal communication skills.
- Ability to effectively translate complex scientific data into reader-friendly content.
???? Project Management:
- Strong time management and multitasking skills.
- Successful completion of a writing exercise (part of candidate evaluation).
✅ Preferred Qualifications
???? Advanced Degree:
- Graduate degree in Life Sciences or a research-related field is preferred.
???? Experience & Knowledge:
- Experience in regulatory, clinical trial, or scientific medical writing.
- Experience in writing Medical Affairs materials (HCP and patient education, slide decks, newsletters, etc.).
- Knowledge of clinical development, pharmacology, and regulatory guidelines.
- Familiarity with therapeutic areas like oncology, immunology, cardiovascular, neuroscience, and endocrinology.
???? Technical Skills:
- Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel).
- Ability to work with document management and scientific communication platforms.
Equal Opportunity Employer
???? At Lilly, we are committed to diversity, inclusion, and equal opportunities. We believe that embracing diverse perspectives fosters innovation and excellence.
???? If you require accommodation to submit your application, please visit our Workplace Accommodation Request page.
???? Join us and be part of a team that is transforming lives through science and innovation!
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