Are you a skilled communicator with a passion for science? Do you enjoy translating complex data into clear, impactful medical content? If yes, then Eli Lilly, a global healthcare leader, is calling you to join its Medical Affairs – Medical Writing team based in Bengaluru.
Whether you’re a recent Pharm.D graduate or a science writer with experience, this is your chance to be part of something bigger — enhancing patient lives through scientific communication.
🌍 About Eli Lilly
Headquartered in Indianapolis, Eli Lilly is a name synonymous with innovation, compassion, and progress. With over a century of experience, the company continues to deliver life-changing medicines and empower healthcare communities across the globe.
What sets Lilly apart is its culture — a harmonious blend of science-driven mission and employee-focused growth. Lilly believes in nurturing talent, supporting diversity, and giving back to society. If you want to contribute to global health while growing in a supportive environment, this is your opportunity.
📌 Job Overview
- 👨⚕️ Role: Medical Affairs – Medical Writing
- 🏢 Organization: Eli Lilly
- 📍 Location: Bengaluru, Karnataka
- 💸 Salary: ₹5 – ₹11 LPA (based on experience)
- 🕐 Experience: 1 to 2 years
- 🎓 Qualification: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, MBBS, Ph.D., M.Tech, or MPH
- 🧪 Domain: Medical Affairs, Scientific Writing
- 📝 Verified Position
🧠 Purpose of the Role
Scientific knowledge is one of the most critical assets at Eli Lilly. The Medical Affairs (MA) team ensures accurate, unbiased, and scientifically valid content reaches all stakeholders — from regulators to patients.
As a Medical Affairs Content Development Specialist, your primary responsibility will be to develop scientific content that informs, educates, and drives healthcare outcomes. You’ll be a bridge between data and decision-making, playing a crucial role across the drug development lifecycle.
🔑 Key Responsibilities
✍️ Content Development & Strategy:
- Draft and finalize regulatory documents supporting clinical trials and product registration.
- Review and analyze scientific data to create compelling, evidence-based documents.
- Conduct kickoff meetings to align writing objectives with stakeholders.
- Build scientific justifications that support regulatory and clinical decisions.
- Collaborate with global teams to develop presentations for internal and external use.
- Maintain document quality through multiple rounds of expert reviews.
📅 Project & Communication Management:
- Take ownership of timelines and deliverables.
- Coordinate with project managers, medical experts, and cross-functional teams.
- Ensure timely completion without compromising on document accuracy.
- Escalate bottlenecks proactively to stakeholders.
📚 Knowledge Enhancement:
- Stay updated with therapeutic area advancements and regulatory guidelines.
- Upgrade communication strategies to match the evolving digital landscape.
- Learn and apply new documentation tools and software.
🤝 Coaching & Collaboration:
- Mentor peers on writing techniques and industry best practices.
- Share learnings across regional and global teams.
- Participate in process improvement discussions to refine writing workflows.
🧾 Required Qualifications & Skills
🎓 Educational Background:
Candidates must hold at least one of the following:
- B.Pharm / M.Pharm
- Pharm.D / MBBS / Ph.D.
- M.Tech / MPH
- B.Sc / M.Sc (Life Sciences, Biotech, Chemistry)
🧠 Experience & Skills:
- 1 to 2 years of experience in regulatory, clinical, or scientific writing.
- Strong written and verbal communication in English.
- Attention to scientific detail and analytical reasoning.
- Time management and the ability to meet tight deadlines.
- Familiarity with industry guidelines (ICH, GPP3, CONSORT).
- Project management basics — planning, execution, stakeholder coordination.
🌟 Why Choose Eli Lilly?
Here’s what makes Lilly a top employer in healthcare:
| Feature | Description |
|---|---|
| 🧪 Innovation Focus | Work on breakthrough therapies for real diseases. |
| 👥 Diverse Culture | Collaborate across geographies and backgrounds. |
| 🌱 Career Growth | Clear learning paths and mentorship opportunities. |
| 💼 Work-Life Balance | Flexible work policies and supportive environment. |
| 💊 Meaningful Work | Contribute to drugs that make lives better. |
📋 Sample Day-in-the-Life:
Imagine this:
- 9 AM: Daily team sync-up on current projects.
- 10 AM: Reviewing new trial data for a document draft.
- 12 PM: Sync meeting with regulatory affairs to finalize timelines.
- 2 PM: Content writing and integrating expert feedback.
- 4 PM: Review internal submission guidelines.
- 5 PM: Submit a presentation draft for medical director approval.
Every day is purposeful, filled with learning and impact.
🎯 Career Opportunities After This Role
Joining as a Medical Writing Specialist opens doors to roles like:
- Medical Affairs Manager
- Senior Medical Writer
- Clinical Document Lead
- Scientific Communication Strategist
- Global Publications Manager
With Lilly’s global footprint, internal mobility is actively encouraged.
📌 Final Thought
This isn’t just a writing job — it’s a mission-driven career in a cutting-edge pharma environment. If you love combining science with storytelling and want to be part of a team that’s improving lives globally, apply to this role today.
You’ll not only grow professionally but also become a vital voice in how scientific truths are shared with the world.
Content Writer
