Clinician, Companion Animal Clinical Development

Responsibilities:
- Design and execute companion animal pharmaceutical and biopharmaceutical clinical development studies in compliance with U.S. CVM/CVB regulatory requirements.
- Lead overall conduct of clinical studies for VMRD companion animal R&D projects, including budget development/management, investigator and site selection, protocol development/writing, study monitoring, data analysis/interpretation, and report writing/technical sections for regulatory dossiers.
- Ensure studies are conducted per applicable SOPs, corporate policies, and regulatory guidelines (e.g., Good Clinical Practice/Good Laboratory Practice).
- Collaborate with clinical and project teams to define/track study status, activities, timelines, outcomes; identify constraints and develop solutions with Project Manager/Team Leader.
- Partner with Regulatory Affairs for protocol approval and support submissions of reports/data to USDA-CVM and/or USDA-CVB (may support EU/other international approvals).

Minimum Qualifications:
- DVM
- 3+ years’ experience in U.S. companion animal private practice
- Experience managing companion animal cases involving therapeutics and/or biologics
- Experience designing or contributing to clinical protocols/research studies

Preferred Qualifications:
- PhD; board certification in a companion animal discipline
- Regulatory knowledge (CVM/CVB), regulatory interactions, dossier authorship, global submissions
- Pharmacovigilance/post-marketing, EDC/CTMS, leadership in matrix organizations, CRO/site management
- Peer-reviewed publications; advanced training (clinical pharmacology/epidemiology/translational medicine)

Compensation & Benefits:
- Base salary range: $105,000–$145,000; short-term and long-term incentives
- Healthcare/insurance day one, 401K with match and profit-sharing, 4 weeks vacation
- Visit zoetisbenefits.com for details