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UCSF
Overview
Coordinate multiple clinical research studies, managing data, specimens, and regulatory documentation. Act as a liaison between departments while ensuring compliance with institutional and regulatory guidelines.
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Compensation
Salary not listed
Posted
10 days ago
The coordinator executes and manages research protocols, overseeing data collection and specimen management for multiple clinical studies. They act as an intermediary between departments and ensure compliance with institutional and regulatory agency policies.
$79,824 - $111,792 / YEAR
11 days ago
The coordinator will recruit, enroll, and retain study subjects while managing research protocols and data collection for multiple clinical studies. They are responsible for maintaining regulatory documents, ensuring IRB approval, and coordinating operations between various departments.
$38 / HOUR
12 days ago
The coordinator manages and executes research protocols for kidney disease patients, including patient enrollment and data collection. Responsibilities include maintaining IRB approvals, managing regulatory documents, and utilizing systems like Apex, Redcap, and OnCore.
$80,000 / YEAR
The coordinator executes and manages clinical research protocols, overseeing data collection, specimen management, and regulatory documentation. They act as an intermediary between departments and ensure compliance with institutional and agency policies.
$65,000 / YEAR
15 days ago
The coordinator manages clinical and translational projects, acting as a link between clinicians, research teams, and regulatory authorities. Key duties include overseeing data and specimen management, maintaining regulatory documents, and ensuring IRB compliance.
17 days ago
Perform entry-level duties to support and coordinate clinical trials, including subject recruitment, data collection, and protocol preparation. Assist in maintaining data quality within study databases and ensuring compliance with research guidelines.
23 days ago
Execute and coordinate research protocols for the GI Oncology program, managing data collection and specimen management. The role involves ensuring regulatory compliance, maintaining databases, and acting as an intermediary between various departments.
$32 - $45 / HOUR
24 days ago
The coordinator executes and manages research protocols for patients with Parkinson's and other movement disorders. Key duties include collecting research data, managing regulatory documents, and coordinating complex clinic visits.
26 days ago
The coordinator will act as the primary recruiter, screening and enrolling participants for a phase 1 HIV prevention clinical trial. Responsibilities include managing study visits, data integrity, IRB requests, and coordinating staff and interns.
1 month ago
Execute and coordinate clinical research protocols in the Department of Neurology, managing data collection and specimen management across multiple sites. Responsibilities include maintaining regulatory documents, managing IRB submissions via the CHR system, and ensuring compliance with institutional and agency policies.
The coordinator will manage clinical research studies focusing on HIV prevention, including participant recruitment, enrollment, and data management. They will also handle IRB submissions, regulatory documentation, and support sample collection for the Hair Analytical Lab.
$38 - $61 / HOUR
The Clinical Research Coordinator manages and executes clinical research protocols for breast oncology trials, overseeing administrative tasks, data integrity, and patient scheduling. They act as a liaison between sponsors and research staff while ensuring compliance with regulatory policies and assisting in patient care.
$40 - $45 / HOUR
The Clinical Research Coordinator manages and coordinates research protocols for pediatric diabetes studies, including participant recruitment and data collection. They oversee regulatory compliance, maintain study documentation, and facilitate communication between clinical staff, families, and investigators.
The coordinator independently manages and executes clinical research protocols focused on liver disease and transplantation. Responsibilities include overseeing data collection, ensuring regulatory compliance, and coordinating study operations under the direction of the Principal Investigator.
$38 - $41 / HOUR
The coordinator executes and manages research protocols, overseeing data collection, specimen management, and regulatory documentation. They act as an intermediary between departments to ensure study integrity and compliance with institutional and agency policies.
The Clinical Research Coordinator manages and coordinates research protocols, ensuring data integrity and regulatory compliance across clinical studies. They act as an intermediary between departments, oversee study results, and assist with staff training and protocol oversight.
The Clinical Research Coordinator will independently manage and execute research protocols for perioperative, critical care, and pain medicine studies. They are responsible for coordinating data collection and ensuring operations align with UCSF and regulatory agency policies.
The incumbent will perform entry-level duties to support and coordinate clinical studies for participants with language difficulties at the UCSF Memory and Aging Center. Responsibilities include recruiting and scheduling subjects, managing study data, preparing protocols, and assisting with clinical trial documentation.
2 months ago
The Clinical Research Coordinator will manage and coordinate clinical research protocols, ensuring compliance with UCSF and regulatory agency policies. Responsibilities include data collection, participant enrollment, database management, and overseeing study operations under the direction of the Principal Investigator.
$34 - $55 / HOUR
