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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
American Addiction Centers
Coordinates clinical and administrative aspects of sponsored clinical trials, including subject recruitment, enrollment, and data collection. Acts as the primary liaison between sponsors and investigators while ensuring protocol adherence and regulatory compliance.
$31 - $46 / HOUR
2 days ago
4 C Medical Technologies
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
$75,000 - $95,000 / YEAR
6 days ago
Terumo
The Clinical Research Coordinator provides administrative and operational support to the Clinical Research and Operations department to ensure adherence to study plans and regulatory standards. Responsibilities include managing study documentation, maintaining the electronic trial master file, and coordinating with clinical sites and vendors.
$44,900 - $61,710 / YEAR
7 days ago
Headlands Research
The CRC manages Phase II-IV clinical studies from initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
Salary not listed
8 days ago
Nira Medical
Perform clinical duties including vital signs, blood draws, and ECGs while managing laboratory specimens. Responsible for accurate data entry into EDC systems and ensuring compliance with GCP, IRB, and HIPAA regulations.
9 days ago
The CRC manages and executes Phase I-IV clinical studies from site initiation to close-out, ensuring compliance with FDA and GCP guidelines. Key duties include conducting subject visits, managing recruitment, and maintaining accurate clinical documentation.
Support clinical trials by preparing study documents, recruiting participants, and conducting patient-facing procedures like vital signs and phlebotomy. Manage study data entry in EDC and CTMS systems while ensuring compliance with FDA and GCP guidelines.
$22 - $27 / HOUR
Coordinate all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. Manage subject visits, recruitment, data entry, and collaboration with investigators and sponsors.
$70,000 - $80,000 / YEAR
The Clinical Research Coordinator will manage and execute Phase II-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaborating with investigators and lab teams to maintain study integrity.
Coordinate all aspects of assigned clinical trials from site initiation through close-out while ensuring patient safety and data quality. Maintain strict compliance with protocols, FDA regulations, and GCP/ICH guidelines through accurate documentation and reporting.
$72,000 - $85,000 / YEAR
The Clinical Research Coordinator manages all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. They are responsible for subject visits, accurate documentation, data entry, and maintaining effective communication with investigators and sponsors.
The Clinical Research Coordinator manages and executes Phase I-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaboration with investigators and sponsors.
Coordinate all aspects of assigned clinical trials from site initiation to study close-out, ensuring compliance with study protocols and regulations. Manage subject recruitment, conduct visits, and maintain accurate documentation throughout the trial process.
American Oncology Network
Responsible for the implementation and management of clinical research studies, including patient coordination and protocol adherence. Tasks include managing study designs, ensuring data integrity, and maintaining regulatory compliance under the supervision of a Principal Investigator.
$20 - $35 / HOUR
11 days ago
Duke Careers
The Clinical Research Coordinator will manage study operations, including recruitment, participant engagement, and regulatory compliance for the Cancer Control and Population Sciences program. They will also ensure data integrity, maintain regulatory documentation, and serve as a liaison between investigators, sponsors, and study participants.
$59,829 - $99,960 / YEAR
13 days ago
Adams Clinical
The Enrollment RA supports the evaluation, triage, and enrollment of clinical trial participants while ensuring compliance with study protocols and regulatory requirements. They perform essential administrative and clinical tasks, including scheduling, data entry, and basic clinical procedures like vital signs and phlebotomy.
$18 - $24 / HOUR
Nova Medical Services
The Clinical Research Coordinator manages the planning and execution of clinical trials, ensuring strict adherence to ICH, GCP, and regulatory guidelines. Key duties include coordinating patient visits, maintaining regulatory documentation, and managing study data entry and verification.
$23 - $25 / HOUR
17 days ago
SerenaGroup Inc
The Clinical Research Coordinator manages day-to-day clinical trial activities, including patient recruitment, screening, and study visit execution. They are responsible for maintaining accurate study documentation and ensuring compliance with FDA and ICH-GCP guidelines.
20 days ago
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
