Clinical Research Associate Jobs in United States

Clinical Research team at St. Jude Children's Research Hospital advances pediatric treatments through rigorous study management. The Clinical Research Associate I/II maintains protocol portfolios, conducts informed consent, abstracts and enters data, prepares regulatory submissions and complex reports, and mentors new staff.

Clinical Research team at Parexel ensures the delivery of clinical studies across the United States. The Senior Clinical Research Associate manages site selection, initiation, monitoring, and closure, conducts remote and onsite visits, and ensures compliance with ICH‑GCP and local regulations while updating study data in CTMS.

Bioethics Program at St. Jude Children’s Research Hospital builds ethical frameworks for pediatric care and research. The Clinical Research Associate II supports data abstraction, case report forms, and informed consent for studies on sickle cell, cancer, and neuromuscular disorders.

Department of Radiology at St. Jude Children's Research Hospital advances pediatric imaging to guide diagnosis and therapy monitoring. The Clinical Research Associate supports clinical research by abstracting, collecting, and entering data, preparing reports, and ensuring protocol compliance, while RN associates also provide patient care and education.

Clinical Monitoring team at Rho drives successful clinical trials by overseeing site management and data integrity. The Clinical Research Associate performs both onsite and remote monitoring, conducts 8-10 site visits per month, and ensures compliance with ICH GCP and FDA regulations.

The Angeles Clinic & Research Institute, part of Cedars-Sinai Medical Center, seeks a Clinical Research Data Associate II to manage data for assigned research studies in Los Angeles. This hybrid role involves designing data collection forms, performing clinical data abstraction, processing data, and producing project reports while ensuring regulatory compliance.

Clinical Research Data Associate II manages data for oncology studies, designs data collection forms, abstracts clinical data, processes and cleans data, produces reports, supports audits, trains staff, and performs basic statistical analysis with biostatisticians.

Clinical Research team at Cook Medical leads the oversight of vendor CRAs and monitoring activities for medical device studies. The role mentors and trains vendor staff, ensures compliance with FDA, ISO-14155 and study protocols, and drives process improvements in monitoring strategy.

IQVIA Early Clinical Development team drives Phase 1 trials across diverse therapeutics. The Senior CRA monitors sites, ensures GCP compliance, tracks enrollment, manages TMF/ISF, and collaborates with cross‑functional teams in Durham, NC, onsite.

Krystal Biotech’s Clinical Operations team in Pittsburgh builds and manages gene‑therapy trials. The Clinical Trial Associate coordinates supply logistics, monitors GCP compliance, and trains site staff while traveling up to 50% of the time.

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.

The Associate Clinical Research Coordinator (CRC1) role within the RESEARCH team coordinates and maintains diverse activities related to clinical cancer research in Kennewick, WA, United States. Day-to-day responsibilities include managing patient eligibility, enrollment, data compilation and submission, study evaluation, quality control, and patient follow-up.

The Pulmonary Research Program at the Cedars-Sinai Women's Guild Lung Institute aims to understand lung disease mechanisms and translate findings to improve patient health. The Clinical Research Associate I supports noncomplex research studies by collecting data, scheduling participants, assisting with IRB submissions, and ensuring regulatory compliance.

Alliance for Clinical Trials in Oncology Foundation (Alliance) conducts large-scale cancer clinical trials to advance treatment and prevention. The Clinical Research Associate supports study start‑up and site management, handling feasibility assessments, eTMF filing, CTMS data entry, and coordination with CROs and investigators.

Clinical Research Associate I at a global medical science company founded in 1995, working on the frontline of communication with project stakeholders to ensure timelines, targets, and standards across clinical research projects in various therapeutic indications. Day-to-day duties include conducting onsite monitoring visits, performing CRF review and source document verification, managing clinical site relationships, and supporting study startup and regulatory submissions.

ADC Diabetes Care at Abbott focuses on innovative diabetes management solutions. The Clinical Research Associate I assists in planning, executing, and managing clinical studies, including site qualification visits, regulatory document collection, device shipment coordination, and trial master file maintenance.

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.

The Clinical Research Associate I at bioMérieux works in parallel with Clinical Trial Managers to manage clinical studies, serving as the primary liaison between bioMérieux and clinical study site personnel for logistical coordination and first-line troubleshooting. Day-to-day duties include coordinating specimen shipping and receiving, resolving data discrepancies with Data Management, providing logistical and regulatory support to sites, and performing related lab duties under close supervisio

Neurology Clinical Trials Team at Georgetown University Medical Center conducts cutting‑edge research on neuroimmunology and neuromuscular disorders. The Clinical Research Associate coordinates seven active trials, schedules patient visits, ensures regulatory compliance, enters data into OnCore/CTMS, and reports adverse events while serving as the primary patient liaison.

The University of South Florida seeks a Clinical Research Associate to oversee regulatory components and participant management for clinical trials in Tampa, FL. This on-site role involves coordinating study visits, ensuring data quality, and maintaining compliance with federal regulations under the direction of the Principal Investigator. The position supports both sponsored and investigator-initiated studies through rigorous protocol adherence.