Clinical Research Associate Jobs in Arizona, United States

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.

The Associate Clinical Research Coordinator - Cancer at Mayo Clinic in Phoenix, AZ coordinates non-therapeutic clinical research protocols under the direction of a principal investigator or supervisor, with possible assistance on complex interventional studies. Day-to-day work includes screening, enrolling, and recruiting participants; scheduling and monitoring research activities; recognizing and reporting adverse events and protocol deviations; collecting, abstracting, and entering data; and h

The Associate Clinical Research Coordinator at Mayo Clinic in Phoenix, AZ, supports non-therapeutic clinical research protocols under the direction of a principal investigator or supervisor. Day-to-day work includes screening, enrolling, and recruiting participants; coordinating schedules and monitoring study activities; collecting and entering research data; and handling administrative and regulatory duties.

Merck seeks a Clinical Research Associate to manage assigned protocols and sites within Immunology, ensuring compliance with ICH/GCP and country regulations. The role involves acting as the primary site contact, performing remote and on-site monitoring, and developing new clinical research territories across designated US locations.

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.

Clinical Research Associate on the Cardiovascular/Vaccine/Infectious Disease team at Merck, responsible for ensuring protocol compliance and site performance across multiple US locations. The role monitors clinical sites, manages relationships, conducts site visits, and oversees data quality and patient safety while collaborating with cross‑functional teams.

Clinical Research team at Merck drives cardiovascular, vaccine, and infectious disease studies. The Clinical Research Associate monitors site compliance, manages study documentation, and builds strong site relationships across the United States.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. As a Senior Clinical Research Associate you will manage site activities for CNS and Oncology studies, conduct initiation visits, ensure regulatory compliance, and support remote monitoring while traveling regionally as needed.

The FSP team seeks a Clinical Research Associate 2 to support clinical trials on the West Coast or in Texas. This role involves comprehensive site monitoring, data integrity verification, and adverse event reporting to ensure participant safety and protocol compliance.

Clinical Research team at Castle Biosciences ensures high‑quality clinical studies through robust quality management. The Internal Quality Assurance Associate supports day‑to‑day QA operations, assists with QMS implementation, develops SOPs, manages document control and LMS processes, and aids internal and external audits to maintain compliance with GCP and regulatory standards.

Clinical Operations at Worldwide Clinical Trials builds and manages global CNS and psychiatry studies. The CRA leads site selection, start‑up, training, and ongoing monitoring, ensuring regulatory compliance and data quality.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for CNS/Psychiatry studies, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely.

Worldwide Clinical Trials, a global CRO, advances clinical research across therapeutic areas including neuroscience and rare diseases. As a Senior Clinical Research Associate you will manage site activities from start-up through closeout, conduct study initiation visits, ensure regulatory compliance, and support contract and budget negotiations, primarily working remotely while traveling regionally on the West Coast.

Join a global clinical research team that has supported the top 50 pharmaceutical companies and 750+ biotechs across 2,700 trials in 100+ countries. As an Assistant Clinical Research Associate, you will perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead, providing support with site preparedness, logistical support to the monitoring process, and assisting with site management and remote monitoring tasks per SOPs and regulatory guidelines.

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 Safety Team at Castle Biosciences ensures participant protection and regulatory compliance for FDA‑regulated LDT, IVD, and medical device studies. The Clinical Research, Clinical Safety Manager establishes and continuously improves safety processes, oversees adverse event management, risk assessments, safety reporting, and regulatory documentation, while partnering with cross‑functional teams to maintain inspection readiness.

Care Access Research team advances community health by conducting clinical studies and delivering advanced health screenings. The Clinical Research Assistant supports patient coordination, specimen processing, and regulatory compliance while performing basic clinical procedures and assisting with recruitment.

Lonnie and Muhammad Ali Movement Disorder Center at St. Joseph's Hospital & Medical Center in Phoenix, Arizona, drives cutting‑edge research on Parkinson’s and movement disorders. The Clinical Research Specialist coordinates study visits, manages informed consent, collects data, and serves as the primary liaison with sponsors and investigators.