Study Director managing animal health product studies at Argenta. Overseeing GLP compliance and coordinating with sponsors for successful project management.
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
Requirements
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
Benefits
Opportunity to work within a growing, global business
Meaningful impact on performance, transformation, and long-term success
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