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ICON plc
Overview
The Clinical Research Nurse I will support the execution of clinical trials by assisting in planning, implementation, and coordination of research activities while conducting patient assessments and administering study treatments. This role involves collecting, recording, and maintaining accurate patient data in eCRFs and collaborating with multidisciplinary teams to ensure efficient study conduct and participant retention.
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Compensation
Salary not listed
Posted
17 days ago
Tulane University
Coordinate day-to-day operations for cardiovascular disease studies, acting as a liaison between patients, investigators, and sponsors. Responsibilities include screening and enrolling patients, ensuring protocol compliance, and managing regulatory documentation.
28 days ago
CentraState Healthcare System
The Research Nurse oversees and directs the clinical course of research participants in clinical trials under the direction of the principal investigator or manager, ensuring strict adherence to local and federal laws and regulations. Key duties involve study implementation, subject recruitment, enrollment, accurate documentation, and acting as the liaison between the sponsor and physician regarding protocol activities.
$48 - $82 / HOUR
1 month ago
Medpace, Inc.
The role involves completing source documents accurately according to protocol and SOPs, and performing blinded independent central review of radiology examinations for clinical studies. Responsibilities also include participating in training, overseeing central readers, and collaborating on technical or radiological concerns.
Profound Research
The Clinical Research Coordinator will manage all clinical trial activities under supervision, ensuring compliance with protocols, laws, and regulations. Key duties include leading trial implementation from start-up to follow-up, training staff, managing documentation, and reporting adverse events.
3 months ago
CenExel
The Nurse Practitioner will provide primary care, assist in the evaluation and treatment of research participants, conduct interviews, and collect/interpret diagnostic data. They must ensure adherence to protocol requirements, protect participant rights, and maintain data integrity according to regulations.
The Nurse Practitioner provides primary care, assists in the evaluation and treatment of research participants, conducts interviews, and collects/interprets diagnostic data. They must ensure adherence to protocol requirements, protect participant rights, and assure data integrity according to regulations.
University Health Partners of Hawaii
The Clinical Trials Research Nurse independently oversees the ethical conduct of oncology clinical trials, coordinating patient care, study visits, and ensuring strict adherence to protocol requirements using sound nursing judgment. This role involves performing protocol-specific clinical tasks, managing data collection, reporting deviations and adverse events, and ensuring patient safety throughout the trial lifecycle.
4 months ago
AXIS CLINICALS LLC
Assist with study operations by ensuring activities occur as scheduled and documents are completed. Tasks include collecting vital signs, distributing meals, and supporting phlebotomists during blood draws.
$16 - $18 / HOUR
K2 Staffing LLC
The Quality Control Associate monitors and performs routine compliance checks on all source data according to protocol requirements and regulatory standards like ICH-GCP and FDA Regulations. Key duties include reviewing source documents for eligibility verification, confirming adherence to organizational policies, and serving as a quality point of contact for sites.
5 months ago
