Research Scientist - Product development
Elanco
August 19, 2026
Remote friendly (Indianapolis, IN)
United States
Clinical Research and Development
Your Role: Clinical Development Scientist – Parasiticides
Responsibilities:
- Lead planning and execution of global clinical programs (pilot and pivotal studies) in compliance with GLP, vGCP, VICH, and applicable regulatory standards.
- Develop clinical development plans; author study protocols and reports; collaborate cross-functionally to deliver on time and at high quality.
- Design and oversee efficacy and target animal safety (TAS) studies with Clinical Development Sciences, Biostatistics, Regulatory Affairs, and external research facilities to support global regulatory approvals.
- Analyze and interpret study data; prepare documentation; support regulatory submissions and presentations to scientific forums.
- Ensure quality assurance and regulatory compliance; contribute to process improvements and advancement of clinical development practices.
Qualifications:
- Education: DVM or Ph.D. in Animal Science (MS with relevant experience considered). Advanced degree in addition to DVM is desirable.
- Skills: Strong project management/organizational skills; excellent written and verbal communication.
Preferred Qualifications:
- Experience interacting with regulatory authorities and supporting product registrations.
- Working knowledge of GCP, GLP, GMP, and global regulatory frameworks.
- Ability to lead/influence cross-functional teams and external research partners.
- Strategic mindset to drive clinical programs and align stakeholders.
- Understanding of R&D processes in animal health or pharmaceutical industries.
Additional Information: Travel 10–20% (potential international). Indianapolis, IN (Hybrid).
Benefits: Multiple relocation packages; two weeklong shutdowns (mid-summer and year-end) plus PTO; 8-week parental leave; 9 Employee Resource Groups; annual bonus; flexible work arrangements; up to 6% 401(k) matching.
Application Instructions: If you don’t meet every requirement, you’re encouraged to apply.
Responsibilities:
- Lead planning and execution of global clinical programs (pilot and pivotal studies) in compliance with GLP, vGCP, VICH, and applicable regulatory standards.
- Develop clinical development plans; author study protocols and reports; collaborate cross-functionally to deliver on time and at high quality.
- Design and oversee efficacy and target animal safety (TAS) studies with Clinical Development Sciences, Biostatistics, Regulatory Affairs, and external research facilities to support global regulatory approvals.
- Analyze and interpret study data; prepare documentation; support regulatory submissions and presentations to scientific forums.
- Ensure quality assurance and regulatory compliance; contribute to process improvements and advancement of clinical development practices.
Qualifications:
- Education: DVM or Ph.D. in Animal Science (MS with relevant experience considered). Advanced degree in addition to DVM is desirable.
- Skills: Strong project management/organizational skills; excellent written and verbal communication.
Preferred Qualifications:
- Experience interacting with regulatory authorities and supporting product registrations.
- Working knowledge of GCP, GLP, GMP, and global regulatory frameworks.
- Ability to lead/influence cross-functional teams and external research partners.
- Strategic mindset to drive clinical programs and align stakeholders.
- Understanding of R&D processes in animal health or pharmaceutical industries.
Additional Information: Travel 10–20% (potential international). Indianapolis, IN (Hybrid).
Benefits: Multiple relocation packages; two weeklong shutdowns (mid-summer and year-end) plus PTO; 8-week parental leave; 9 Employee Resource Groups; annual bonus; flexible work arrangements; up to 6% 401(k) matching.
Application Instructions: If you don’t meet every requirement, you’re encouraged to apply.