JobsSr Scientist - Global Regulatory Project Lead - Farm Animal
Sr Scientist - Global Regulatory Project Lead - Farm Animal
ElancoSr Scientist - Global Regulatory Project Lead - Farm Animal
ElancoLocation
Indianapolis, IN
Type
Full-time
Posted
6/20/2026
Compensation
$118,000 - $197,000 per year
Undergraduate with 5+ Years of Experience
Approval 98.6%·Filings 69·New hires 31·
✓ Established Sponsor
·FY 2025Job description
As the Global Regulatory Project Lead at Elanco, you will be a key contributor in guiding the regulatory strategy for innovative farm and companion animal products. This role involves serving as the regulatory expert on global project teams and leading negotiations with regulatory agencies like the U.S. Food and Drug Administration. You will collaborate with various internal stakeholders to ensure successful submissions in the U.S., European Union, and other key markets. Your work will directly impact the development of products that enhance animal health and well-being.
Requirements
- A Master’s degree or higher in veterinary medicine, biology, infectious diseases, immunology, animal science, or a related field.
- At least 10 years of relevant experience in the animal health industry, with direct regulatory affairs experience in veterinary pharmaceuticals.
- Demonstrated experience leading direct submissions and negotiations with regulatory agencies, particularly the U.S. Food and Drug Administration's Center for Veterinary Medicine.
- Proven ability to serve as the primary regulatory expert on cross-functional project teams in a global environment.
Responsibilities
- Guide the design and development of the global regulatory strategy for development projects, focusing on CVM/FDA submissions.
- Serve as the dedicated regulatory subject matter expert on development teams, representing the regulatory viewpoint and providing risk/benefit evaluations.
- Act as the primary point of contact for and lead direct engagements with regulatory agencies, including pre-submission meetings and negotiations.
- Partner with R&D to develop and implement clinical trial submission plans, ensuring alignment with the overall regulatory strategy.
- Collaborate with internal stakeholders to provide technical leadership on Quality, Safety, and Efficacy sections for regulatory submissions.
- Proactively identify and communicate project-specific regulatory risks and opportunities to the development team and leadership.
Benefits
- Employees at Elanco are often offered competitive compensation with annual bonus and equity eligibility, retirement plans (including a U.S. 401(k)), and comprehensive health coverage—medical, dental, vision, company-paid life and disability—and even pet insurance. Time-off and flexibility typically include generous PTO, U.S. mid-year and year-end paid shutdown weeks, parental leave, and flexible/remote work options. Employees also benefit from strong development programs (onboarding, course libraries, mentorship, nine ERGs, and tiered leadership programs) that support both professional growth and community involvement.
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