Are you passionate about advancing healthcare through scientific communication? Eli Lilly and Company, a global healthcare leader headquartered in Indianapolis, Indiana, is hiring a Senior Associate/Lead Global Scientific Communications (GSC) Regulatory Writing for our team in Bengaluru, India.
This role offers a unique opportunity to contribute to life-changing medicines by crafting high-quality regulatory documents that support clinical development and product registration. Join us to unite caring with discovery and make life better for people worldwide.
Application Details
- Location: Bengaluru, Karnataka, India
- Application Method: Send your resume to careers@lilly.com with the subject line “GSC Regulatory Writing Application – Bengaluru”
- Application Deadline: May 15th, 2025
- Website: careers.lilly.com
Notes:
- Candidates must complete a writing exercise as part of the evaluation process.
- Submit an updated resume, academic certificates, and relevant experience letters.
- For accommodation requests, complete the form at Lilly Workplace Accommodation.
Why Join Eli Lilly?
Founded in 1876, Eli Lilly is a global pharmaceutical leader with a presence in over 120 countries, dedicated to discovering and delivering innovative medicines. Our Bengaluru office is a hub for scientific and technical expertise, fostering a collaborative environment where employees thrive.
Rated 4.3/5 for work-life balance on Glassdoor, Lilly is committed to diversity, inclusion, and employee development. Join us to work on impactful projects in clinical development and regulatory affairs, supported by a culture that puts people first.
Job Position: Senior Associate/Lead Global Scientific Communications (GSC) Regulatory Writing
We are seeking a skilled professional to lead the development of regulatory documents, ensuring scientific accuracy and compliance with global standards.
Job Details
- Experience: 3–8 years in technical/regulatory scientific writing
- Qualification: Bachelor’s degree in a scientific, health, communications, or technology-related field (Graduate degree with a research component or in Life Sciences preferred)
- Location: Bengaluru, India
Key Responsibilities
Content Strategy and Execution
- Collect and evaluate data from multiple sources to create cohesive content strategies for writing projects
- Plan, write, edit, and coordinate regulatory documents supporting clinical development and product registration
- Conduct document initiation meetings to align authoring teams
- Build scientific-based rationales for complex/strategic documents
- Ensure data accuracy, consistency, and clarity across related documents
- Coordinate quality checks and expert reviews, incorporating feedback to finalize documents
- Work across multiple document types and therapeutic areas
Project and Stakeholder Management
- Lead the writing process with effective project management to meet timelines
- Build and communicate credible project timelines, mitigating risks to delivery
- Collaborate with internal teams and external experts to ensure smooth document development
- Communicate project status to stakeholders and escalate issues as needed
- Manage relationships with vendors and alliance partners when required
Knowledge and Skills Development
- Maintain and enhance knowledge of therapeutic areas, compounds, and regulatory guidelines
- Stay updated on ICH and publication guidelines
- Develop expertise in clinical planning, submission strategies, and regulatory responses
- Adapt to evolving technology and platforms to meet audience needs
Knowledge Sharing
- Provide coaching and technical guidance to team members
- Share best practices and contribute to process improvements
- Offer expertise in document management systems and database tools
Required Skills and Qualifications
| Category | Details |
|---|---|
| Education | Bachelor’s degree in scientific, health, communications, or tech field (Graduate degree preferred) |
| Experience | 3–8 years in technical/regulatory scientific writing |
| Technical Skills | Proficiency in word processing, tables, graphics, spreadsheets, and presentations |
| Regulatory Knowledge | Strong understanding of ICH, FDA, and global regulatory guidelines |
| Soft Skills | Excellent communication, interpersonal, and project management skills |
| Preferred Expertise | Clinical pharmacology, therapeutic areas (e.g., oncology, neuroscience), or clinical trial processes |
Why This Role?
- Global Impact: Contribute to regulatory documents that enable life-changing medicines.
- Diverse Projects: Work across therapeutic areas like oncology, cardiovascular, or immunology.
- Career Growth: Enhance your skills through coaching, knowledge sharing, and exposure to global teams.
- Inclusive Culture: Join a company committed to diversity and equal opportunities.
How to Apply
To apply for the GSC Regulatory Writing position, follow these steps:
- Prepare Your Documents: Update your resume, highlighting your regulatory writing experience, and gather academic certificates and experience letters.
- Complete the Writing Exercise: Be prepared to participate in a writing exercise as part of the evaluation process.
- Email Your Application: Send your documents to careers@lilly.com with the subject line “GSC Regulatory Writing Application – Bengaluru.”
- Include Key Details: Mention your total experience, current CTC, expected CTC, and notice period.
- Research Lilly: Visit careers.lilly.com to learn about our mission and scientific communications expertise.
- Prepare for the Interview: Be ready to discuss your experience with regulatory documents, ICH guidelines, or project management in clinical development.
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Why Bengaluru?
Bengaluru, India’s biotech and innovation hub, offers a vibrant ecosystem for Life Sciences professionals. Lilly’s Bengaluru office is strategically located, providing access to cutting-edge infrastructure and a collaborative work environment. Learn more about Bengaluru’s biotech industry.
Contact Information
For inquiries or to apply, reach out to:
- Email: careers@lilly.com
- Accommodation Requests: Workplace Accommodation Form
- Website: careers.lilly.com
Equal Opportunity: Lilly is dedicated to diversity and inclusion, ensuring equal opportunities for all candidates, including those with disabilities. We do not discriminate based on age, race, color, religion, gender, sexual orientation, or any other legally protected status.
Don’t miss this chance to join a global healthcare leader and contribute to life-changing medicines. Apply by May 15th, 2025, and shape the future of scientific communications with Eli Lilly!
