Design and execute companion animal pharmaceutical and biopharmaceutical clinical development studies in compliance with U.S. CVM/CVB regulatory requirements
Job Summary
Design and execute companion animal pharmaceutical and biopharmaceutical clinical development studies in compliance with U.S. CVM/CVB regulatory requirements.
Lead the overall conduct of clinical studies, including budget management, investigator selection, protocol development, study monitoring, data analysis, and report writing.
Collaborate with Clinical and Project Teams to define and track study status, activities, timelines, and outcomes, and partner with Regulatory Affairs for protocol approval and regulatory submissions.
Matching Summary
Design and execute companion animal pharmaceutical and biopharmaceutical clinical development studies in compliance with U.S. CVM/CVB regulatory requirements.
Skills & Requirements
Must-have
Companion animal pharmaceutical studies
Biopharmaceutical clinical development studies
U.S. CVM/CVB regulatory compliance
Protocol development and writing
Study monitoring and data analysis
Nice-to-have
Expertise in companion animal medicine
Collaboration with cross-functional teams
Global regulatory submissions experience
Familiarity with pharmacovigilance
Key Requirements
Doctor of Veterinary Medicine (DVM)
3 years experience in U.S. companion animal private practice
Experience managing clinical cases with therapeutics/biologics
Experience designing clinical protocols or research studies