Argenta is currently looking to fill the role of Study Director at our Oakland, NE location.
Key Responsibilities
- Approve and sign study protocol
- Ensure objectives meet regulatory requirements
- Coordinate with Sponsors and Quality Assurance
- Delegates tasks accordingly during the course of the study but retails full responsibility
- Ensures the study follows GLP and study protocol, overseeing animal care, sample collection and data recording
- Addresses deviations and ensures proper documentation
- Review and interpret results ensuring the scientific validity of conclusions
- Writes, approves and signs the final study report
- Ensures 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
Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through a strong culture, great benefits, and growth opportunities.
