Clinical Research Associate Jobs in Kansas, United States

Clinical Monitoring team at Rho Inc, dedicated to advancing clinical trials through rigorous site oversight and data integrity. The CRA conducts both onsite and remote monitoring visits, ensures protocol compliance, and mentors junior staff while collaborating with clinical sites and internal stakeholders.

Clinical Operations team at AbbVie conducts global clinical trials to develop innovative medicines. The Clinical Research Associate II monitors investigative sites, ensures protocol compliance, data quality, and regulatory adherence while training site staff and managing investigator payments.

Clinical Research team at AstraZeneca conducts global clinical trials to bring innovative medicines to patients. The Clinical Research Associate manages study delivery at assigned sites, collaborates with monitors and local delivery teams, and ensures compliance with ICH/GCP, AZ procedures, and local regulations.

Clinical Research team at AstraZeneca conducts global clinical studies to advance innovative medicines. The Clinical Research Associate ensures study sites are initiated, monitored, and closed according to ICH/GCP standards, collaborates with local study delivery teams, and manages data quality and regulatory compliance.

Clinical Research team at AstraZeneca conducts field‑based monitoring of clinical studies to ensure high‑quality data and patient safety. The CRA manages study sites, oversees initiation, monitoring, and closure activities, and collaborates with local study delivery teams to meet protocol timelines.

Novotech Clinical Research team ensures trial participants' rights and data integrity across studies. The Clinical Research Associate builds site relationships, prepares regulatory documents, monitors sites onsite or remotely, and verifies data compliance with ICH GCP and sponsor SOPs.

Clinical Affairs team at Phagenesis Ltd drives the development of life‑saving neurogenic dysphagia therapies. The CRA oversees day‑to‑day operational aspects of assigned studies, conducts site visits, ensures compliance with GCP and FDA regulations, and collaborates with cross‑functional teams to resolve issues and support audit readiness.

Clinical Research Associate I at Mount Sinai Health System supports psychiatry clinical trials from Phase I to Phase IV. The role manages study documents, monitors milestones, and coordinates site recruitment and supplies. Based in the United States, the position requires on‑site presence at the Mount Sinai campus.

Novotech Clinical Research Team: The Clinical Research Associate (CRA) ensures trial participants’ rights and wellbeing are protected while guaranteeing accurate, complete data. The role manages site relationships, monitors compliance with ICH GCP and local regulations, and coordinates recruitment and data verification.

Novotech’s Clinical Research Associate (CRA) team safeguards trial participant rights and ensures data integrity across global studies. The CRA manages site relationships, monitors compliance with ICH GCP and local regulations, and coordinates recruitment and data verification.

Responsible for site selection, initiation, monitoring, and closure of clinical studies, ensuring compliance with ICH‑GCP, AZ SOPs, and local regulations. Manages study supplies, data quality, and regulatory submissions, and collaborates with local MSLs and study teams to drive site performance and inspection readiness.

AstraZeneca seeks a Clinical Research Associate to manage study delivery at centers, collaborate with monitors, prepare and close sites per AZ procedures, ensure quality commitments, and support senior CRA tasks. Requires 1.5+ years CRA experience in cardiovascular, metabolic, respiratory or immunology, Bachelor’s in Life Science, fluency in English, ICH/GCP knowledge, basic GMP/GDP, local regulations, medical knowledge of AZ therapeutic areas, drug development basics, study management, monitoring, data handling, 50-70% travel, and strong communication, analytical, and teamwork skills.

Clinical Research Associate in oncology drives study delivery at local sites, ensuring compliance with ICH/GCP and local regulations. The role involves monitoring, initiating, and closing clinical trials, collaborating with monitors and study teams, and maintaining quality standards.

Clinical Research Associate, Sponsor Dedicated at IQVIA is responsible for monitoring and site management across multiple U.S. locations. The role requires performing site monitoring visits—selection, initiation, monitoring, and close‑out—according to the contracted scope of work and Good Clinical Practice (GCP).

Field Based Clinical Research Associate at AstraZeneca responsible for delivering studies at allocated centers, collaborating with Monitors and Local Study Delivery Team, preparing, initiating, monitoring, and closing centers per AZ documents and ICH/GCP, ensuring quality and quantity commitments, and potentially advancing to Lead CRA/Senior CRA/Site Liaison roles.

Clinical Research Team responsible for overseeing multi‑phase clinical trials across pharmaceutical, biotech, and medical device studies. The Senior Clinical Research Associate conducts site monitoring visits, ensures protocol and GCP compliance, and resolves data discrepancies while collaborating with investigators and cross‑functional project teams.

Clinical Research Operations at Novartis drives site-level execution of Phase I‑IV trials to deliver high‑quality data and bring innovative therapies to patients faster. The Senior CRA leads assigned sites, builds strong relationships, conducts remote and on‑site monitoring, and collaborates with cross‑functional teams to ensure compliance, patient safety, and timely trial milestones.

Clinical Research Team responsible for advancing clinical trials across Phase I–IV studies. The Senior Clinical Research Associate builds strong site relationships, conducts on‑site and remote monitoring, and ensures compliance with ICH/GCP guidelines while driving data quality and patient‑centered outcomes.

Clinical Research team at Novartis drives innovative therapies by overseeing Phase I‑IV trials across the United States. The Senior Clinical Research Associate leads site relationships, conducts on‑site and remote monitoring, ensures compliance with ICH/GCP, and resolves risks to deliver high‑quality data.

Clinical Research team advancing in vitro diagnostics and medical devices to improve patient outcomes worldwide. The Senior Clinical Research Associate oversees end‑to‑end trial execution, conducts site monitoring, manages regulatory documentation, and ensures data integrity across multiple studies.