Hybrid Study Director – Americas CRO

Posted 9 hours ago

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About the role

  • 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

Job title

Study Director – Americas CRO

Job type

Experience level

Lead

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

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