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Systimmune
Overview
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
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Compensation
$90,000 - $130,000 / YEAR
Posted
9 days ago
American Addiction Centers
Provides administrative and operational support to the Alzheimer's Disease Research Center, splitting time between administrative and clinical cores. Key tasks include managing patient appointments, maintaining research logs, and supporting regulatory and financial processes.
$22 - $33 / HOUR
11 days ago
Adams Clinical
Provide foundational operational and administrative support for clinical trials, including participant screening, scheduling, and clinical procedures. Maintain accurate ALCOA+-compliant documentation and perform data entry into EDC systems to ensure audit readiness.
$22 - $25 / HOUR
13 days ago
Arizona Center for Cancer Care
The Clinical Research Assistant provides essential administrative and operational support for clinical research studies, focusing on document management, regulatory submissions, and scheduling under the supervision of the clinical program manager. This role involves assisting CRCs and investigators by ensuring study documentation is accurate, organized, and compliant with regulatory standards to facilitate efficient trial conduct.
Salary not listed
2 months ago
US Foot & Ankle Specialists
The Clinical Research Coordinator will independently manage and execute clinical trials, overseeing day-to-day study operations, regulatory compliance, patient coordination, and data management according to protocol and guidelines. Key duties include managing the full study lifecycle from start-up to closeout, ensuring compliance, and coordinating with investigators, sponsors, and the IRB.
Civia Health
The Nurse Practitioner will conduct study visits, including medical assessments and physical exams, while partnering with principal investigators to ensure quality, safety, and regulatory compliance across clinical trials. Responsibilities also involve engaging participants empathetically, managing adverse events, and maintaining accurate documentation in source records and EDC systems.
ALLIANCE CLINICAL LLC
The Assistant Clinical Research Coordinator will support the execution of clinical trials by assisting with participant screening, visit coordination, accurate data collection in CRFs and EDC systems, and maintaining essential study documentation. This role also involves supporting informed consent, monitoring adverse events, coordinating specimen handling, and ensuring strict adherence to study protocols and regulatory guidelines.
$20 - $26 / HOUR
3 months ago
