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Expect scenarios on global regulatory pathfinding for farm-animal assets, managing multi-region timelines, and working with R&D and quality stakeholders. Review Elanco’s animal-health focus and recent public innovation/earnings news.
Strong fit if you have senior regulatory project leadership in animal health or related life sciences and prefer structured, multi-market coordination over pure lab science.
As Sr Scientist – Global Regulatory Project Lead – Farm Animal, you would coordinate cross-functional regulatory work for farm-animal products: align submission plans, track global health-authority requirements, and keep development and commercial partners synchronized on timelines, dossiers, and risk decisions.
Strengthen regulatory science for veterinary/farm-animal products, global submission strategy, project leadership, and cross-functional communication. No specific certifications were provided for this posting.
The listing marks remote as no; treat it as U.S.-based with site details to confirm in interview.
Elanco is an animal-health company (founded 2000) focused on products and innovation for animals, including farm-animal areas.
No verified salary, review scores, or Glassdoor/Indeed figures were provided—do not assume compensation from this enrichment.
Website: elanco.com/en-us
Public cache only — not an employee review.
Elanco (NYSE: ELAN) is hiring a Sr Scientist – Global Regulatory Project Lead – Farm Animal to steer regulatory strategy for breakthrough animal health products across the United States. If you thrive at the intersection of veterinary science and agency negotiation, this role puts you at the heart of a global innovation pipeline. About the Role As the Global Regulatory Project Lead, you'll work as a senior individual contributor and the go-to regulatory authority on global project teams. From the earliest stages of development, you will shape strategy for novel farm and companion animal products and lead direct discussions with authorities such as the U.S. Food and Drug Administration's Center for Veterinary Medicine (CVM). The position calls for someone who can manage intricate agency interactions and align partners across R&D, Sales and Marketing, Supply Chain, Manufacturing & Quality, Finance, and Technical Services to secure approvals in the US, EU, and other first-wave markets. Key Responsibilities Shape and execute the global regulatory strategy for development programs, centered on CVM/FDA submissions. Act as the dedicated regulatory subject matter expert, offering risk/benefit assessments that inform project direction. Serve as the lead contact for engagements with agencies such as CVM and the European Medicines Agency (EMA), including pre-submission meetings and negotiations. Work alongside R&D to build and deliver clinical trial submission plans aligned with the broader regulatory approach. Provide technical guidance on the Quality, Safety, and Efficacy components of submissions. Surface and communicate regulatory risks and opportunities to teams and leadership. Uphold all local and global policies, including quality frameworks, the Code of Conduct, and HSE standards. Qualifications Master's degree or higher in veterinary medicine, biology, infectious diseases, immunology, animal science, or a related discipline. A minimum of 10 years in the animal health industry, including hands-on regulatory affairs work in veterinary pharmaceuticals. Track record of leading direct submissions and negotiations with regulators, ideally the FDA's CVM. Demonstrated success as the primary regulatory expert on cross-functional global teams, with standout communication and influencing skills. Preferred: experience across both farm and companion animal products, global first-wave registrations including the EU, novel regulatory pathways, risk management…
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