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Arizona Liver HealthNew
Overview
Coordinate clinical research trials by recruiting participants, performing clinical procedures like phlebotomy and vitals, and managing study data. Ensure strict adherence to regulatory guidelines, maintain study documentation, and collaborate with sponsors and internal staff.
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Compensation
$28 - $36 / HOUR
Posted
New
Evolution Research Group
The Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They are responsible for ensuring protocol adherence, managing subject recruitment, and maintaining accurate regulatory documentation under the direction of the Principal Investigator.
Salary not listed
9 days ago
The Clinical Research Coordinator manages the overall implementation, organization, and coordination of clinical trials at the site. They ensure protocol adherence, manage subject recruitment, and maintain accurate regulatory documentation under the direction of the Principal Investigator.
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
The Clinical Research Coordinator II manages the implementation and coordination of clinical trials, ensuring compliance with protocols and regulatory standards. They are responsible for subject recruitment, screening, informed consent, and maintaining accurate study documentation.
13 days ago
UT Southwestern Medical Center
Coordinate a portfolio of high-complexity neurological surgery trials, including investigator-initiated and industry-funded studies. Manage regulatory compliance, subject recruitment, data collection, and patient safety monitoring according to protocol guidelines.
22 days ago
Coordinate a portfolio of high-complexity neurological surgery trials, including investigator-initiated and industry-funded studies. Manage regulatory compliance, subject recruitment, data collection, and the execution of study procedures according to protocol.
23 days ago
CenExel
Provides direct support to Clinical Research Coordinators by maintaining patient charts and preparing visit materials. Responsible for data entry, conducting basic assessments like blood pressure, and coordinating with study participants and vendors.
$18 - $22 / HOUR
24 days ago
St. Joseph Hospital & Medical Center
Manage and execute clinical trials by coordinating subject visits, collecting data, and ensuring strict adherence to protocols. Act as a key liaison between sponsors, investigators, and study subjects to maintain data integrity and patient safety.
$24 - $36 / HOUR
CHARLOTTE BEHAVIORAL HEALTH CARE INC
The CRF APRN provides evaluation and treatment to adults and youth in an inpatient behavioral health and substance use setting. They work collaboratively with the treatment team to conduct psychiatric evaluations, prescribe medications, and assist with treatment planning.
$150,650 - $165,755 / YEAR
Cedars-Sinai
Coordinates and implements complex clinical research studies by managing data collection, participant scheduling, and IRB submissions. Serves as a primary contact for sponsors and provides training to junior staff to ensure protocol compliance.
Assist in the coordination and implementation of noncomplex clinical research studies through data collection and participant scheduling. Support regulatory compliance by assisting with IRB submissions and maintaining study supplies.
$24 - $33 / HOUR
28 days ago
The Research Assistant provides direct support to Clinical Research Coordinators by managing patient charts, preparing visit materials, and performing data entry. They also conduct basic clinical assessments and maintain study-specific supplies while adhering to strict regulatory guidelines.
Nationwide Children's Hospital
Manages clinical study elements including recruitment, enrollment, and day-to-day management following ICH/GCP guidelines. Responsible for collecting research data, processing human specimens, and maintaining regulatory binders.
1 month ago
La Clinica de Familia Inc.
The Chronic Care Specialist supports high-risk patients in navigating the healthcare system and collaborates with multidisciplinary teams to manage chronic care and transitions. They act as a resource for clinic staff and perform nursing duties within their professional license scope.
$16 - $22 / HOUR
Beth Israel Lahey Health
The Clinical Research Coordinator manages the administration of multiple research studies, ensuring protocol adherence and regulatory compliance. Key duties include recruiting and screening participants, collecting study data, and maintaining communication with sponsors and investigators.
$19 - $31 / HOUR
CHOC
The CT Technologist II provides computed tomography and diagnostic radiography services to pediatric patients according to physician orders. This role involves administering contrast, adhering to low-dose radiation practices, and serving as a resource for other technologists.
$39 - $65 / HOUR
The coordinator independently manages clinical study activities, including patient screening, informed consent, and accurate data collection. They ensure strict compliance with FDA and IRB regulations while reporting study progress and accrual data to staff.
$28 - $48 / HOUR
The coordinator manages clinical study activities, including patient screening, informed consent, and accurate data collection. They ensure compliance with FDA and IRB regulations while reporting study progress and accrual data.
$24 - $40 / HOUR
The Research Assistant I provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and ensuring accurate data entry. They also assist with participant visits, conduct basic assessments, and facilitate communication between study stakeholders.
