Explore Regulatory Writing roles (Associate/Senior Associate/Lead) at Lilly, Bangalore. Join a global healthcare leader in drug development. Apply today for a rewarding career in scientific communications!
Eli Lilly and Company is a global healthcare leader dedicated to discovering life-changing medicines. Headquartered in Indianapolis, USA, Lilly operates in multiple countries, including India, with a strong presence in Bangalore. The company focuses on innovation, patient care, and community support through philanthropy and volunteerism.
At Lilly, employees work on cutting-edge drug development, ensuring regulatory compliance and scientific accuracy. The Regulatory Writing team plays a crucial role in preparing documents for global health authorities, making this a high-impact career opportunity.
Detailed Job Description
Job Title:
Associate/Senior Associate/Lead – Regulatory Writing
📍 Location: Bangalore, Karnataka, India
📌 Category: Research & Development
🕒 Job Type: Full-Time (Regular)
🔍 Job ID: R-87544
Purpose of the Role:
The Regulatory Writing team ensures high-quality, accurate, and compliant documents for regulatory submissions. This role involves:
- Developing protocols, amendments, informed consent forms (ICFs), and regulatory dossiers
- Collaborating with cross-functional teams to align on scientific content
- Ensuring timely, clear, and compliant documentation for global health authorities
Key Responsibilities:
1. Content Strategy & Execution
✔ Plan, write, and edit regulatory documents (protocols, clinical study reports, etc.)
✔ Ensure data accuracy, consistency, and compliance with regulatory standards
✔ Coordinate expert reviews and finalize documents
2. Project & Stakeholder Management
✔ Lead document development timelines and mitigate risks
✔ Communicate project status to internal and external stakeholders
✔ Collaborate with medical, clinical, and regulatory teams
3. Knowledge & Skills Development
✔ Stay updated on therapeutic areas, regulatory guidelines, and industry trends
✔ Adapt to different document types and therapeutic areas
4. Knowledge Sharing
✔ Mentor junior writers and share best practices
✔ Contribute to process improvements in regulatory writing
Eligibility & Requirements
✅ Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field
✅ Experience in regulatory/scientific writing (clinical protocols, ICFs, etc.)
✅ Strong scientific, analytical, and communication skills
✅ Ability to work in a fast-paced, cross-functional environment
(A writing exercise is required as part of the evaluation process.)
Benefits of Working at Lilly
🌟 Global Exposure – Work with international teams
🌟 Career Growth – Opportunities for advancement
🌟 Work-Life Balance – Flexible policies
🌟 Health & Wellness – Comprehensive benefits
🌟 Inclusive Culture – Equal opportunity employer
