Animal Health Clinical Research Associate III

Argenta

Clinical Research Associate for animal health at Argenta, coordinating GCP protocols and site compliance. Requires extensive experience in clinical trials and strong analytical skills.

Posted 5/29/2026full-timeRemote • Kansas • 🇺🇸 United StatesJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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

Benefits

Comp & perks

Health insurance
Strong culture
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

GCPclinical trial monitoringdata trackingQuality Control (QC)data query resolutionelectronic data capture (EDC)study protocol complianceadverse event trackingstudy record reviewanalytical skills

Soft Skills

attention to detaildependabilityflexibilitymultitaskingtime managementrelationship buildingcommunicationcollaborationproblem-solvinginterpersonal skills