Argenta, US Clinical is currently looking for an experienced Clinical Research Associate to join our team. You may be an excellent fit for our team if you have the following: - 8+ years clinical trial monitor experience within a Clinical Research Organization or major Animal Health pharmaceutical company - proven experience in GCP late phase clinical trials in animal health - attention to detail and analytically driven - dependability, flexibility and ability to multitask and manage time effectively Our Clinical Research Associates add value through the following responsibilities: - Coordinates and conducts GCP and study protocol training at study sites and assures training is documented - Builds rapport with study site staff to assure compliance with the protocol, applicable regulatory and guidance documents, SOPs, and all study activities - Assists in reviewing the study records and all study notebooks to ensure contents are current and complete - Assists in providing tracking and Quality Control (QC) of data as required and assists with responses to QA audits - Evaluates Investigators and assists with 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 - Monitors assigned study sites through review of electronic data capture (EDC) systems, faxed, emailed, and paper documentation. - Serves as the liaison between Argenta US Clinical and study site personnel - Facilitates clarifications, corrections, and data query resolution with study sites or data management personnel - Tracks adverse events (AE's) encountered in clinical studies and ensures all serious AEs and non-serious AEs are documented and communicated appropriately to the Project Manager and Sponsor - Learns to assist with facilitates clarifications, corrections, and data query resolution with study sites or data management personnel - Builds relationships with key individuals and contributors in the organization and beyond Job Requirements include: - Minimum of 8 years' experience in an animal health research role, Monitor and Clinical Research Associate positions preferred - Experience in Good Clinical Practice (GCP) data management, quality control, and/or quality assurance preferred - Collaborative working style. Lead and motivate people through influence across all levels and functions of the organization - Ability to look for creative solutions to resolve complex issues - Strong technical writing ability - Results oriented and driven - Strong communication and listening skills - Well organized and analytically driven - Willingness to travel, expected to travel nationally 40 to 60% Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through strong culture, great benefits, and opportunity for growth. This role is subject to a DEA background check as well as a pre-employment drug screen and/or physical.