Clinical Research Associate Jobs in Kansas, United States

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

IQVIA seeks a Clinical Research Associate to ensure sites conduct studies and report data per protocol, regulations, and sponsor requirements. The role involves performing site monitoring visits, managing recruitment plans, and maintaining regulatory documentation like the Trial Master File.

Clinical Research Associate on Merck's Oncology team, responsible for ensuring compliance and performance of clinical trial protocols across assigned sites. The role conducts site monitoring, manages regulatory documentation, and collaborates with cross‑functional teams to support study start‑up, execution, and close‑out.

IQVIA’s Clinical Research Associate team drives site monitoring and management to ensure compliance with GCP and ICH guidelines. The role conducts site visits, manages recruitment plans, administers protocol training, and maintains Trial Master File documentation across multiple U.S. locations.

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

Clinical Research Associate on IQVIA’s Sponsor Dedicated team, ensuring sites conduct studies per GCP and ICH guidelines. The role monitors visits, drives recruitment, trains sites, evaluates quality, tracks regulatory submissions, maintains TMF, and manages financials.

IQVIA’s Clinical Research team drives site monitoring to ensure compliance with GCP and ICH. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files. Based in Overland Park, KS with additional sites in Durham, NC; Parsippany, NJ; and Carlsbad, CA, the position is on-site with a hybrid travel component.

Animal Health Clinical Research Associate III at Argenta works in Shawnee, KS, supporting GCP late‑phase animal health trials. The role coordinates site training, monitors data quality, and collaborates with project managers to ensure protocol compliance.

Clinical Research team at IQVIA ensures study sites adhere to protocols and regulatory standards. The Senior Clinical Research Associate conducts site monitoring visits, manages recruitment plans, and oversees documentation and financial aspects of trials.

Perform site monitoring visits, manage study progress, ensure compliance with GCP/ICH, maintain TMF/ISF, generate reports, support recruitment, handle financials, and collaborate with study teams.

IQVIA’s Clinical Research team drives site monitoring and data integrity for clinical trials. The Associate conducts GCP‑compliant site visits, manages recruitment plans, and ensures accurate CRF submission.

Fortrea's FSP team is seeking a Clinical Research Associate 2 for the Central Region to deliver high-standard clinical trial monitoring and participant care across a remote territory spanning multiple states. Day-to-day, the role covers full-cycle site monitoring, pre-study and initiation visits, CRF review and query resolution, SAE reporting, and registry management, with 8-10 on-site days per month.

IQVIA’s Clinical Research Associate team drives site monitoring and management to ensure compliance with GCP and ICH guidelines. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files while coordinating with study teams.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

Fortrea is seeking Experienced CRA 2s to lead and support its Full Service Outsourcing team across major US hub locations. In this role, you will apply clinical judgement to monitor clinical trial sites, ensure participant safety and data integrity, and respond to emergencies per clinical research standards.

Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Associates (CRA 1) for Oncology, CAR T, or Ophthalmology trials. The role involves site monitoring, data integrity verification, SAE reporting, and supporting study site operations across Central or West coast US hubs or Montreal, Canada.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

Clinical Research at Grene Vision Group supports human subject studies and ensures high‑quality trial operations. The Coordinator manages daily trial activities, from participant recruitment and data collection to quality assurance and IRB reporting, while adhering to GCP guidelines.