Study Director - Americas CRO
Argenta, Shawnee, KS, United States
Argenta is seeking a Study Director to join our Americas CRO leadership team. The ideal candidate will play a critical role in our leadership team and will act as the single point of control and accountability for assigned studies.
Key Responsibilities
- Approve and sign study protocol
- Ensure objectives meet regulatory requirements
- Coordinate with Sponsors and Quality Assurance
- Delegate tasks accordingly during the course of the study but retain full responsibility
- Ensure the study follows GLP and study protocol, overseeing animal care, sample collection and data recording
- Address deviations and ensure proper documentation
- Review and interpret results ensuring the scientific validity of conclusions
- Write, approve and sign the final study report
- Ensure all raw data are archived properly
About You
- Advanced degree in a scientific discipline.
- 10+ years experience in animal health product development, or veterinary clinical study project management.
- Proven experience managing cross functional teams
- Thorough knowledge of practical experience in GLP protocols, Final Study Reports and Study Master Files
- Collaborative working style and the ability to lead and motivate people at all levels and across multiple functions within the organization
- Proven affinity with Animal Health
- Excellent attention to detail and scientific judgement