Offer summary
Qualifications:
DVM/VMD or equivalent veterinary training, Experience in Regulated Pharmaceutical Animal Health, Working knowledge of veterinary regulatory frameworks, Advanced scientific writing skills, Fluency in English.Key responsabilities:
- Plan, execute, and report clinical studies
- Ensure compliance with veterinary regulations
- Select and manage subcontractors (CROs)
- Author protocols and regulatory documents
- Facilitate cross-functional collaboration for drug development