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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
10 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
12 days ago
Adams Clinical
Provide foundational operational and administrative support for clinical trials, including participant screening, scheduling, and clinical procedure execution. Maintain accurate ALCOA+-compliant documentation and assist with data entry into EDC systems and regulatory binder management.
$24 - $27 / HOUR
14 days ago
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
M3USA
The Clinical Research Assistant supports daily clinical trial activities, ensuring protocol compliance and data quality under the guidance of site leadership. Key duties include managing clinical supplies, performing phlebotomy, and documenting participant data in source records and EDC systems.
Salary not listed
17 days 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.
2 months ago
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.
