Offer summary
Qualifications:
5+ years in R&D in Animal Health, DVM or equivalent degree, Experience in cross-functional teams, Proficient in Microsoft Office, Clinical development experience in biologics.
Key responsabilities:
- Develop and execute clinical strategies for regulatory approvals.
- Oversee design and execution of clinical studies.
- Ensure high-quality execution according to plans and regulations.
- Collaborate with Discovery and CMC for candidate progression.
- Monitor study execution and troubleshoot issues.