Eli Lilly and Company, a global healthcare leader headquartered in Indianapolis, Indiana, is hiring for Associate/Senior Associate/Lead – Regulatory Writing positions in its Research & Development division at the Bengaluru, Karnataka, India facility.
With a mission to unite caring with discovery, Lilly develops life-changing medicines and supports communities worldwide. Join a Great Place to Work certified organization (rated 3.7/5 on AmbitionBox for job security) to make a meaningful impact in regulatory scientific communications
About Eli Lilly and Company
Founded in 1876, Eli Lilly operates in 18 countries with a workforce of over 35,000, focusing on oncology, diabetes, immunology, and neuroscience. Its Bengaluru R&D center drives innovation in clinical development and regulatory affairs, contributing to Lilly’s global portfolio of 70+ medicines.
Employees praise job security (3.9/5) and skill development (3.8/5), but work-life balance (3.5/5) can be challenging due to project deadlines and high expectations.
Job Details: Associate/Senior Associate/Lead – Regulatory Writing
- Job ID: R-87544
- Category: Research & Development
- Job Type: Full-Time, Regular
- Work Location: Bengaluru, Karnataka, India
- Posted: May 15, 2025
- Application Contact: careers.lilly.com
Purpose
The Scientific Communications Associate – Regulatory role involves leading the development of high-quality regulatory documents (e.g., protocols, amendments, ICFs) to support clinical development and product registration. This position collaborates with cross-functional teams to ensure accurate, timely, and compliant communication with regulators, healthcare professionals, and stakeholders.
Primary Responsibilities
Content Strategy and Execution:
- Collect and evaluate data from multiple sources to create cohesive content strategies
- Plan, write, edit, and finalize regulatory documents, ensuring clarity, accuracy, and conciseness
- Build scientific rationale for complex documents and ensure data consistency across related documents
- Coordinate expert reviews, incorporate feedback, and perform quality checks
- Prepare presentations and manage vendor relationships as needed
Project and Stakeholder Management:
- Lead document development with effective project management to meet timelines
- Build credible project timelines, mitigate risks, and escalate issues as needed
- Communicate project status clearly to stakeholders
Knowledge and Skills Development:
- Maintain expertise in assigned therapeutic areas, compounds, and regulatory guidelines
- Adapt across document types, therapeutic areas, and compounds
- Stay updated on industry trends, competitors, and publication guidelines
Knowledge Sharing:
- Coach team members by sharing technical expertise and best practices
- Contribute to process improvements and provide database/tool expertise
- Network across functions to enhance collaboration
Minimum Qualifications
- Education: Bachelor’s degree in a scientific, health, communications, or technology-related field
- Experience: Demonstrated experience in technical/regulatory scientific writing
- Skills:
- Strong communication and interpersonal skills
- Proficiency in medical, scientific, or technical writing
- Successful completion of a writing exercise (required during evaluation)
- Preferred:
How to Apply
- Application Process: Submit your resume via careers.lilly.com. Complete the required writing exercise during the evaluation process.
- Accommodation: For disability-related accommodations, fill out the form at careers.lilly.com/workplace-accommodation.
- Contact: For inquiries, use the career portal or email careers@lilly.com.
Documents Required:
- Updated resume
- Copies of educational certificates
- Experience certificates (if applicable)
- Aadhaar Card and PAN Card (for Indian applicants)
Verified by Trusted HRs
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Why Join Eli Lilly?
Lilly’s Bengaluru R&D center offers exposure to global clinical development and regulatory affairs, with opportunities to work on innovative therapies. Employees benefit from:
- Skill Development: Hands-on experience with regulatory documents and advanced tools (3.8/5)
- Job Security: High stability in a global leader (3.9/5)
- Culture: Collaborative, patient-centric environment
- Benefits: Competitive salaries (average ₹1,558,999 annually in India), health insurance, and philanthropy opportunities However, tight project timelines may challenge work-life balance (3.5/5). Lilly is committed to diversity and inclusion, ensuring equal opportunities for all.
Why Bengaluru?
Bengaluru is India’s pharmaceutical and R&D hub, offering a vibrant ecosystem for career growth. Lilly’s office in Electronic City is accessible, though commuting may be required due to traffic.
Important Notes
- Eligibility: Candidates with regulatory writing experience and a scientific background. Writing exercise mandatory.
- Disclaimer: Lilly does not charge fees for job applications or request money for employment. Report suspicious requests to www.cybercrime.gov.in.
- Note: Candidates interviewed in the last 6 months need not reapply. Expect a high-pressure, deadline-driven role with significant learning opportunities.
Don’t miss this chance to join Eli Lilly and Company! Apply by visiting careers.lilly.com and contribute to life-changing medicines in Bengaluru
