Clinical Development Scientist,Companion Animal Health Job Indianapolis Indiana USA,Research/Development

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your Role:

Clinical Development Scientist, Companion Animal Health As a Clinical Development Scientist, you will be a key member of the team responsible for delivering Elanco's innovation pipeline to our customers. Your role is pivotal in bringing innovative vaccines and therapeutic products for companion animals to market, from initial study design through regulatory approval. Reporting to the Clinical Leader, you will have the opportunity to design and execute studies that advance animal well-being and support Elanco’s mission.

Your

Responsibilities:

Lead the planning, implementation, and reporting of high-quality clinical studies (pilot and pivotal) for new companion animal vaccines and therapeutics, ensuring compliance with global regulatory standards (USDA, GLP, vGCP, VICH).
Author comprehensive study protocols and final reports, select and manage contract research facilities, and oversee all aspects of study execution to meet project objectives.
Develop and execute strategic clinical development plans, fostering strong collaboration with cross-functional teams including R&D, Regulatory Affairs, Quality Assurance, and Marketing.
Partner with Regulatory Affairs to prepare and present clinical data for submission to global regulatory agencies, directly contributing to product approvals.
Drive quality and compliance within clinical programs, contribute to process improvements, and maintain current knowledge of industry trends and scientific advancements.

What You Need to Succeed (minimum qualifications):

Education:A DVM or Ph.D. in a relevant scientific discipline; OR an M.S. in a relevant discipline.
Experience:A minimum of 5 years of direct experience in veterinary product development required for candidates with an M.S. degree. Proven experience in the clinical development of health products, including hands‑on involvement in planning and executing studies.
Top 2 skills:Proven ability to contribute to clinical program strategy and translate scientific objectives into executable study designs; and strong collaboration and communication skills to effectively drive projects in a cross‑functional, team‑oriented environment.

What will give you a competitive edge (preferred qualifications):

Significant direct experience in the companion animal health vaccine or pharmaceutical industry.
An advanced degree (e.g., Ph.D.) in addition to a DVM.
Deep working knowledge of and direct experience with global regulatory standards (e.g., USDA, vGCP, GLP, VICH) and regulatory authorities.
Demonstrated success in managing external partnerships, such as contract research organizations (CROs).
Proven ability to take a lead role in driving a clinical program vision and cultivating innovation from development through to regulatory approval.

Additional Information:

Travel:10-20% Domestic and possible International
Location:Global Elanco Headquarters
- Indianapolis, IN
- Hybrid Work Environment

Don’t meet…