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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.
Job Responsibility:
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
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