Clinical Research Associate Jobs in United States

Cell Therapy Site Management & Monitoring team ensures clinical study sites deliver high-quality data and compliance across New York and New Jersey. The Clinical Research Associate monitors site initiation, conduct and closure, performs source data verification, manages study supplies and updates CTMS, while training investigators and ensuring regulatory adherence.

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 at IQVIA Biotech partners with biotech companies to accelerate clinical development. Responsible for onsite monitoring of clinical trial sites, ensuring compliance with GCP, ICH, and sponsor protocols.

Alliance for Clinical Trials in Oncology Foundation's Operations team drives large-scale cancer clinical research. The Clinical Research Associate supports site management, feasibility assessments, eTMF and CTMS oversight, and regulatory compliance across studies.

This role oversees clinical trial site monitoring and management, ensuring compliance with GCP and ICH guidelines. Responsibilities include conducting site visits, evaluating site performance, maintaining trial documentation, and collaborating with study teams to support recruitment and data quality.

Clinical Research Associate at NAMSA supports medical device studies by ensuring GCP compliance, coordinating site monitoring, conducting qualification and close‑out visits, serving as primary contact for site queries, communicating performance trends, supporting study start‑up and document quality, providing training, maintaining master files, tracking enrollment and adverse events, attending meetings, reporting progress, supporting safety activities, and preparing regulatory submissions.

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.

Clinical Research team at CTTX Health focuses on advancing innovative neuroscience therapies through rigorous clinical trials. The Clinical Research Associate conducts site initiation, monitoring, and close-out visits, verifies study data, and collaborates with site staff to resolve challenges and ensure protocol compliance.

Clinical Research team at Extremity Care oversees clinical trial operations to ensure data integrity and regulatory compliance. The Clinical Research Associate monitors multiple study sites, develops monitoring plans, tracks enrollment, and prepares reports while coordinating with investigators and internal teams.

Clinical Operations team at AstraZeneca conducts global clinical studies. The Clinical Research Associate monitors site activities, ensures compliance with ICH‑GCP, conducts remote and onsite visits, and drives enrollment and data quality.

In House Clinical Research Associate

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 supports cancer studies by enrolling patients, managing data entry, and ensuring regulatory compliance. The role involves verifying consent, monitoring protocol adherence, reporting adverse events, maintaining study binders, coordinating sponsor visits, and resolving data queries.

Veracyte Clinical Research team drives execution of clinical research programs focusing on wet lab testing for cancer diagnostics. The Clinical Research Associate oversees sample receipt, processing, testing, and reporting, partners with R&D and CLIA‑certified labs to ensure assay compliance, and supports protocol development and data quality monitoring.

Clinical Research team at AstraZeneca conducts global clinical studies to develop innovative medicines. As a Field Based Clinical Research Associate you will manage study sites, ensure compliance with ICH/GCP guidelines, and collaborate with local study delivery teams to meet quality and timeline goals.

Clinical Research team at AstraZeneca drives global clinical studies to bring innovative medicines to patients. The Field Based Clinical Research Associate manages study delivery at assigned sites, overseeing initiation, monitoring, and closure while ensuring compliance with ICH/GCP and local regulations.

Clinical Research Team at AstraZeneca conducts global clinical studies to develop innovative medicines. The Field Based Clinical Research Associate manages site delivery, prepares, initiates, monitors, and closes study centers while collaborating with local teams to meet quality and timeline commitments.

Clinical Research team at AstraZeneca drives the development of innovative medicines by overseeing study execution across therapeutic areas. As a Field Based Clinical Research Associate you will manage the preparation, initiation, monitoring and closure of study sites, collaborating with monitors and local delivery teams to meet quality and timeline commitments.

Clinical Research Associate at Ortho-Clinical Diagnostics, Inc. in Athens, OH. The role writes clinical protocols for beta-site and formal studies, sets up and monitors IVD trials, ensures data accuracy, site compliance, and manages trial master files. Onsite work in a lab/warehouse environment with flexible hours.

Clinical Research Associate, Sponsor Dedicated at IQVIA supports clinical trials by monitoring sites, ensuring compliance with GCP and ICH guidelines, and managing study documentation. The role involves conducting site initiation, monitoring, and close‑out visits, coordinating recruitment plans, and tracking regulatory submissions.