Clinician, Companion Animal Clinical Development

Responsibilities

• Lead the overall conduct of clinical studies in support of Veterinary Medicine Research & Development (VMRD) companion animal R&D projects, including: Budget development and management
• Investigator and site selection
• Protocol development and writing
• Study monitoring
• Data analysis and interpretation
• Report writing and preparation of technical sections for regulatory dossiers
• Ensure studies are conducted in compliance with applicable requirements, including Standard Operating Procedures (SOPs), corporate policies, and regulatory guidelines (e.g., Good Clinical Practice and Good Laboratory Practice).
• Collaborate with Clinical and Project Teams to define and track study status, activities, timelines, and outcomes. Identify resource, timeline, and/or budget constraints and work with the Project Manager and Project Team Leader to develop appropriate solutions.
• EDUCATION AND EXPERIENCE

Requirements

• Doctor of Veterinary Medicine (DVM)
• Minimum of 3 years of experience in U.S. companion animal private practice
• Experience managing clinical cases involving therapeutics and/or biologics in companion animals
• Experience designing or contributing to clinical protocols or research studies
• PhD
• Board Certification in a companion animal discipline
• Working knowledge of U.S. regulatory requirements for animal health products, including Center for Veterinary Medicine (CVM) and Center for Veterinary Biologics (CVB) guidelines
• Experience in companion animal clinical development within the Animal Health industry Experience interacting with regulatory agencies (e.g., technical section authorship or direct communication with CVM/CVB)
• Prior authorship of regulatory dossiers supporting product approvals
• Experience with global regulatory submissions (EU, Canada, Australia, etc.)
• Familiarity with pharmacovigilance and post-marketing surveillance requirements
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS)
• Demonstrated leadership of cross-functional teams in a matrixed organization
• Experience managing CROs and external study sites
• Publication record in peer-reviewed veterinary journals
• Advanced training in clinical pharmacology, epidemiology, or translational medicine
• This position is also eligible for short-term incentive compensation
• This position is also eligible for long-term incentives
• Visit zoetisbenefits.com to learn more.
• Full time
• Regular
• Colleague
• Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.

Benefits

Additional Information

Zoetis is currently seeking a Companion Animal Clinical Development Clinician to join our team. In this role, you will design and execute companion animal pharmaceutical and biopharmaceutical clinical development studies in compliance with U.S. CVM/CVB regulatory requirements. You will deliver pilot and pivotal clinical studies that support product registrations and provide expertise in companion animal medicine and study conduct to research and development phase projects.

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