Veterinary Clinical Research Associate

Preparation of study protocols, amendments, deviations, data capture forms, electronic data capture systems, test article documentation, and study reports. Execute and lead multiple CAE Bios studies simultaneously from coordinating animal and study supply shipments through report finalization, including interpretation of data, summaries and analysis, and study archiving.Collaborate with multiple internal partner groups to plan, coordinate, conduct, analyze, and report studies. Conduct training of Investigators and other study site personnel. Serve as the principal communication link between the Sponsor and study sites. Maintain study files in accordance with SOPs and regulatory requirements. Manage data management processes including paper and electronic data capture, overseeing data management plans, data import and review, tracking, and data verification/validation utilizing electronic tools and centralized data management systems. Provide clinical updates to project teams and sub-teams.  This may include scribing meeting minutes to provide to project team leaders and project team members.  Assist with or coordinate animal-related study activities (i.e., clinical sampling, test material administration, and clinical observations). May include minimal animal handling.