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.

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.

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.

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.

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.

Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies.

To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines. May assist in complex (i.e. interventional, therapeutic, greater than minimal risk) studies with direction but does not have overall responsibility for these studies.

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.

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

The FSP team at Covance is seeking a Sr. CRA 2 to provide high-standard clinical trial care and respond to emergency situations based on clinical research standards. Day-to-day responsibilities include all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaising with vendors, and other duties as assigned.

The Sr. CRA II - General Medicine - East Coast or Mid-West role supports the Full Service Outsourcing team at Covance, reporting within the Fortrea Inc. organization. You will lead and support clinical trial operations by performing all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits.

Clinical Research Coordinator with 1+ year experience in interventional trials, skilled in protocol execution, patient coordination, and regulatory compliance. Proven ability to manage study visits, maintain accurate data, and foster relationships with sponsors and investigators.

Clinical Services at Iterative Health drives the acceleration of clinical research for GI and hepatology therapies. The CRC‑RN coordinates daily trial activities, manages recruitment, data entry, and investigational drug accountability, ensuring compliance with GCP and sponsor protocols.

Clinical Research Recruitment Specialist supports patient enrollment for ongoing trials. Frontline role connecting potential participants to research opportunities.

Avacare, a Site Management Organization (SMO) backed by IQVIA, seeks Clinical Research Coordinators to manage diverse clinical trials in Gilbert, AZ. CRCs handle patient recruitment, informed consent, regulatory documentation, site audits, and hands-on clinical procedures across 2–6 trials. This fully on-site role offers broad exposure to multiple therapeutic areas and a collaborative team environment.

Clinical Research Coordinator at Thermo Fisher Scientific manages day-to-day operations of clinical trials in Tucson, Arizona, USA. You will conduct ongoing clinical trials involving patients or healthy volunteers, complete paperwork to capture data per study protocol, and ensure subject safety, understanding, and cooperation. You will engage in site operations including recruitment, enrollment, and retention, provide training to junior team members, and act as lead coordinator for certain studi

Avacare is a Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. CRCs manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish, including patient recruitment, informed consent, regulatory documentation, and site audits.

Organized Clinical Research Assistant skilled in data entry, patient recruitment, phlebotomy, and CTMS. Supports trial operations, maintains charts, manages supplies, and facilitates clinic flow across multiple sites.