Study Director - Americas CRO
On-siteOakland, Nebraska, United States
Job Summary
Approve and sign study protocols while ensuring objectives meet regulatory requirements. Coordinate with sponsors and quality assurance, delegating tasks during the study while retaining full responsibility. Oversee animal care, sample collection, and data recording to ensure strict adherence to GLP protocols and study masters. Address deviations, ensure proper documentation, and review results to guarantee scientific validity of conclusions. Write, approve, and sign the final study report, ensuring all raw data are archived properly. This role requires an advanced degree and 10+ years in animal health product development or veterinary clinical study project management. Based in Oakland, NE, the position offers full-time employment with competitive compensation and benefits.
Required Qualifications
- 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
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