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Orlando HealthNew
Overview
Develop and implement administrative strategies to manage clinical trials and coordinate large-scale research studies. Responsibilities include assessing patient eligibility, monitoring adverse reactions, and ensuring adherence to FDA and protocol guidelines.
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Compensation
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UTHealth HoustonNew
Assists with the conduct and management of human subject research projects, including participant recruitment and data collection. Responsible for maintaining databases, preparing progress reports, and supporting grant proposals and regulatory submissions.
Mass General BrighamNew
Coordinate and run study visits involving neuroimaging and biological sample collection for infection-associated health conditions. Manage IRB compliance documents, screen potential participants, and assist with data processing and analysis.
$21 - $29 / HOUR
UVA HealthNew
Coordinate oncology clinical trials by recruiting, screening, and enrolling participants while ensuring protocol compliance and high-quality data collection. Maintain accurate documentation and collaborate with multidisciplinary research teams to support the advancement of cancer research.
$28 - $81,500 / HOUR
The coordinator will recruit, screen, consent, and enroll participants across multiple cancer clinical trials while building relationships with study participants. Key duties include coordinating study visits, collecting high-quality data, maintaining accurate documentation, processing specimens, tracking adverse events, and ensuring protocol compliance.
$28 - $82 / HOUR
Arizona Liver HealthNew
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.
$28 - $36 / HOUR
Mass General Brigham
The Clinical Research Coordinator supports oncology clinical trials by enrolling eligible patients and scheduling all protocol-mandated tests. Responsibilities include coordinating patient appointments, processing tissue and blood samples, and maintaining communication with enrolled participants.
$29 / HOUR
2 days ago
Manages cardiovascular clinical trials, including subject recruitment, enrollment, and the maintenance of regulatory documentation. Performs clinical tests such as phlebotomy and EKGs while managing research data and biological samples.
$20 - $29 / HOUR
The Clinical Research Coordinator will assist with clinical research studies, including recruiting and consenting patients, collecting data, and performing clinical tests. They will also manage IRB protocols and support various research projects related to military service-related conditions.
The coordinator will assist with clinical research studies by recruiting, evaluating, and consenting patients, collecting and organizing patient data, and scheduling study visits. Key duties also involve performing clinical tests like phlebotomy and EKGs, and maintaining study documentation and data integrity.
The coordinator assists with clinical research studies by recruiting, evaluating, and consenting patients while collecting and organizing study data. They are also responsible for performing clinical tests like phlebotomy and EKGs and maintaining regulatory documentation.
University of Virginia
Coordinate all aspects of complex clinical research projects from start-up through archiving, including patient recruitment and regulatory compliance. Manage multiple trials simultaneously while collaborating with physicians and sponsors to ensure audit-ready documentation.
The Research Coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests like phlebotomy and EKGs. They also ensure study compliance, maintain regulatory binders, and prepare data for analysis.
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
Cleveland Clinic
Coordinate the implementation and conduct of human subject research projects, including complex trials and regulatory documentation. Serve as a liaison between investigators and research personnel while ensuring protocol compliance and effective data management.
The coordinator manages clinical research studies on depression, focusing on participant recruitment, screening, and the administration of assessments. They are also responsible for data collection, maintaining regulatory binders, and contributing to scholarly manuscripts.
Evolution Research Group
The Assistant Clinical Research Coordinator supports the collection, documentation, and analysis of clinical research data for Phase I-IV trials. They perform clinical tasks including venipuncture and ECGs while ensuring study protocols and patient safety guidelines are followed.
Iterative Health
The Clinical Research Coordinator manages daily clinical trial activities, including patient recruitment, protocol adherence, and clinical procedures like blood draws and IV administration. They also ensure data integrity, maintain study documentation, and act as the primary point of contact for study participants.
The Clinical Research Coordinator I supports and coordinates daily clinical trial activities, including administratively and clinically managing industry-sponsored trials, problem-solving, and ensuring protocol adherence. Key duties involve leading patient recruitment, scheduling visits, conducting procedures like blood draws and injections, and dispensing study medication.
UVA Health
The coordinator will manage multiple complex clinical trials from start-up through archiving, including patient recruitment and regulatory documentation. They will collaborate with physicians and sponsors to ensure trials are conducted according to FDA and NIH requirements.
3 days ago
