Eli Lilly Hiring for Regulatory Writing / Associate in Bengaluru
Are you a regulatory writing professional seeking a career with a globally recognized pharmaceutical company? Eli Lilly and Company is inviting applications for multiple positions in Regulatory Writing, including Associate, Senior Associate, and Lead roles. The job openings are at the company’s Research & Development center in Bengaluru, Karnataka, India.
This is an excellent opportunity to work with a company that has been at the forefront of healthcare innovation for nearly 150 years. Eli Lilly Hiring for Regulatory Writing
About Eli Lilly and Company
Founded in 1876, Eli Lilly is a leading global healthcare company headquartered in Indianapolis, Indiana, USA. With operations in over 18 countries and a global workforce of 35,000+ employees, the company focuses on delivering innovative treatments across key therapeutic areas, including oncology, neuroscience, diabetes, and immunology. Eli Lilly Hiring for Regulatory Writing
The Bengaluru R&D center plays a vital role in Lilly’s global operations, driving clinical development and regulatory support for its expanding portfolio of more than 70 medicines.
Position Overview
Roles Available:
- Associate – Regulatory Writing
- Senior Associate – Regulatory Writing
- Lead – Regulatory Writing
Job ID: R-87544
Department: Research & Development
Job Type: Full-Time, Regular
Work Location: Bengaluru, Karnataka, India
Application Mode: Online via careers.lilly.com
Posted Date: May 15, 2025
Purpose of the Role
The role involves developing high-quality scientific and regulatory documents that support the clinical development and registration of new therapies. As part of the Scientific Communications team, selected candidates will collaborate with cross-functional teams to create precise, impactful, and regulatory-compliant documentation. Eli Lilly Hiring for Regulatory Writing
Key Responsibilities
Content Strategy and Document Development
- Create and manage content strategy based on clinical data and regulatory guidelines
- Draft, revise, and finalize critical regulatory documents including:
- Study protocols and amendments
- Informed Consent Forms (ICFs)
- Investigator brochures
- Clinical Study Reports (CSRs)
- Ensure consistency of data and messaging across multiple documents
- Perform document quality reviews and manage feedback from scientific and regulatory teams
- Support vendor and stakeholder presentations as needed
Project and Team Collaboration
- Lead writing projects with clearly defined timelines and deliverables
- Provide regular updates to project teams and escalate challenges when necessary
- Manage review cycles and ensure timely submissions to global regulatory authorities
- Eli Lilly Hiring for Regulatory Writing
Subject Matter Expertise
- Maintain knowledge in assigned therapeutic areas and regulatory writing practices
- Adapt quickly to new compounds, document types, and regulatory changes
- Monitor industry trends, competitors, and publication standards
Mentorship and Process Optimization
- Share technical expertise with junior writers and support team development
- Contribute to SOP improvements, templates, and writing best practices
- Foster collaboration across global scientific communication functions
Candidate Profile
Minimum Qualifications
- Education:
- Bachelor’s degree in Life Sciences, Health Sciences, Communications, or a technology-related field
- Experience:
- Demonstrated experience in regulatory or scientific writing
- Experience in authoring or supporting preparation of clinical trial documents
Skills Required
- Strong written and verbal communication
- Excellent scientific reasoning and understanding of clinical data
- Attention to detail and ability to handle high-volume documentation
- Familiarity with ICH, EMA, and FDA regulatory standards
- Successful completion of a writing exercise is required during the hiring process
Preferred Qualifications
- Advanced degree (Master’s or Ph.D.) with a research background
- Prior experience in oncology, neuroscience, or clinical pharmacology
- Experience working with clinical development or regulatory submissions (CTD, protocols, CSRs, etc.)
Why Join Eli Lilly?
Working at Eli Lilly means being a part of a mission-driven organization that combines compassion with scientific excellence. Here’s why you should consider applying: Eli Lilly Hiring for Regulatory Writing
- Career Growth: Learn from industry experts and get hands-on experience in global regulatory processes
- Job Stability: Rated 3.9/5 for job security on AmbitionBox
- Learning Opportunities: Continuous learning through projects and cross-functional exposure
- Company Culture: Patient-centric, inclusive, and focused on innovation
- Compensation and Perks: Competitive salary packages (average ₹15.5 LPA), health insurance, paid leaves, and philanthropic initiatives
Note: Work-life balance may be demanding due to tight project deadlines, rated 3.5/5 by employees. However, the learning and career advancement opportunities make it a worthy investment in your future. Eli Lilly Hiring for Regulatory Writing
How to Apply
Interested candidates must apply online through the official Eli Lilly careers portal:
Application Checklist:
- Updated Resume
- Educational Certificates
- Experience Letters (if applicable)
- Aadhaar and PAN Card (mandatory for Indian applicants)
Evaluation Process:
- Shortlisted candidates will be required to complete a writing assessment as part of the selection process
- Final rounds may include technical interviews and HR discussions
Accessibility and Accommodations
Candidates with disabilities who require assistance during the application process can request accommodations via the Workplace Accommodation form available at the career site. For other queries, contact: careers@lilly.com Eli Lilly Hiring for Regulatory Writing
Important Notes
- No application fees are charged by Eli Lilly
- Report any fraudulent activity to www.cybercrime.gov.in
- Applicants who have appeared for an interview in the last 6 months need not reapply
- This is a high-responsibility role and may involve strict deadlines
Bengaluru – A Pharma and R&D Hub
Lilly’s R&D facility in Electronic City, Bengaluru, is located in one of India’s most vibrant pharma corridors. With access to top talent, global collaborations, and a growing ecosystem, Bengaluru offers the perfect backdrop for professionals looking to advance in the regulatory and clinical development space. Eli Lilly Hiring for Regulatory Writing
Conclusion
This is a rare opportunity to join a global leader in healthcare and contribute to scientific communications that impact lives worldwide. If you have a regulatory writing background and a passion for delivering accurate and impactful documentation, apply now to Eli Lilly and Company and grow with one of the most respected names in pharma. Eli Lilly Hiring for Regulatory Writing
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