Experience in Good Clinical Practice (GCP) data management, quality control and/or quality assurance is preferred Experience with medical/veterinary terminology Prior Clinical Research Associate I role or equivalent experience and training Experience working with EDC systems (Electronic Data Capture) is a plus Position requires significant computer skills including the ability to use Microsoft Word, Excel, PowerPoint, and Adobe Acrobat The employee must possess a valid driver's license and proper travel documentation i.e., passport, and have the ability to travel Excellent oral and written communication skills Ability to take an assertive approach when needed to keep sites on track with training, documentation, and query resolution A collaborative working style to be able to lead and motivate people at all levels and across all functions in an organization Strong analytical thinking and problem-solving skills Capable of working in a changing environment and under pressure Supports organizational goals and objectives aligned to strategic and/or operations plans. Learns to evaluate Investigators and assists with the selection of appropriate sites to conduct clinical studies Collaborates with the study Project Manager to assure study sites selected meet the needs of the study protocol Participates in monitoring of assigned study sites through review of electronic data capture (EDC) systems, faxed, emailed, and paper documentation Coordinates and travels to study sites to conduct pre-study site evaluations, study initiation, interim monitoring, and study close out visits Assists in verifying owner consent, existence and maintenance of source documents, and inventory of Investigational Veterinary Product/Control Veterinary Product (IVP/CVP) at study sites Maintains an updated study site personnel listing Reviews medical records and identifies discrepancies (demographics, medical history, visits/procedures including unscheduled, adverse events, con meds, etc.).