Clinical Research Associate Jobs in Arizona, United States

Clinical Research team at Merck conducts immunology trials, ensuring protocol compliance and patient safety. The CRA manages site relationships, performs remote and onsite monitoring, and oversees regulatory documentation across multiple US locations.

Clinical Research Operations at Merck conducts cardiovascular, vaccine, and infectious disease trials. The Clinical Research Associate monitors site performance, ensures compliance with ICH/GCP, manages documentation, and supports site selection and expansion.

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 at Mass General Brigham supports clinical studies by collecting patient data, maintaining records, and ensuring protocol compliance. The role involves recruiting participants, conducting interviews, performing phlebotomy, and assisting with regulatory submissions.

Clinical Research team at NAMSA, the premier provider of MedTech development solutions. The associate ensures human subject protection, GCP compliance, and regulatory adherence while coordinating site monitoring, documentation, and training across studies.

Clinical Research team at NAMSA supports global MedTech product development by overseeing study protocols, data collection, and regulatory compliance. The Associate coordinates site activities, monitors trial progress, and ensures accurate documentation throughout the study lifecycle.

Medical Affairs – Clinical Research team at Kuros Biosciences focuses on advancing bone healing through rigorous clinical trials and regulatory compliance. The Clinical Research Associate manages study tracking, conducts site monitoring visits, ensures GCP/ICH adherence, and supports audits across multiple US territories.

Clinical Research Associate on the Phase I team at Covance, ensuring high‑standard care for trial participants and rigorous site monitoring. The role manages all site activities, from initiation to close‑out, and handles data integrity, SAE reporting, and vendor coordination.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

PPD Development, LP’s Clinical Research Associate team drives global clinical trials, ensuring protocol compliance and data integrity. The role monitors investigator sites, conducts risk‑based monitoring, and manages documentation across 100+ countries.

Thermo Fisher Scientific seeks a Clinical Research Associate (Level II) to monitor clinical trials across multiple U.S. sites. The role blends on‑site and remote visits, applying risk‑based monitoring, ICH‑GCP compliance, and data accuracy checks (SDR, SDV, CRF).

Clinical Research team at Merck conducts ophthalmology trials across the United States. The Senior Clinical Research Associate manages site relationships, ensures protocol compliance, and leads monitoring activities both remotely and on‑site, mentoring junior CRAs.

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.

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.

Worldwide Clinical Trials' Clinical Operations team drives innovative clinical research across therapeutic areas, including CNS/Oncology. The Senior Clinical Research Associate manages site activities from start-up to closeout, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations, primarily working remotely with regional travel on the West Coast.

NAMSA’s Clinical Research team drives global MedTech safety by overseeing clinical trials from start‑up to close‑out. The Senior CRA ensures GCP compliance, coordinates site monitoring, manages study documents, and supports audits and safety reporting.

Novartis Clinical Research team seeks a Senior CRA to lead site monitoring for Phase I‑IV trials across the U.S., ensuring data integrity and regulatory compliance. The role manages site initiation, ongoing monitoring, and data query resolution while coordinating with project managers and medical liaisons.

Senior Clinical Research Associate at SystImmune, a leading biopharma focused on innovative cancer therapeutics. The role drives site management, monitoring, and data quality for oncology trials, ensuring compliance with ICH‑GCP and regulatory standards.

EASA Center for Excellence (E4CE) team at OHSU-PSU School of Public Health provides clinical training, technical assistance, and consultation for early psychosis and substance use interventions. The role designs and delivers training, evaluates program effectiveness, and integrates feedback to improve services for youth and young adults.