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UTHealth HoustonNew
Overview
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.
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Compensation
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Posted
New
UTHealth Houston
Coordinate day-to-day operations for clinical research studies, including participant recruitment, enrollment, and data management. Assist with regulatory submissions, budget preparation, and the creation of research papers and reports.
4 days ago
University of Rochester
This role coordinates human subject research activities within the Department of Urology, focusing on screening, consenting subjects, maintaining documentation, and managing data collection according to research protocols. The specialist ensures research activities adhere to institutional policies, IRB requirements, and study protocols while coordinating with the Principal Investigator and other study team members.
$21 - $30 / HOUR
8 days ago
The Research Coordinator III manages clinical trials in Movement Disorders, overseeing participant recruitment, data collection, and regulatory compliance. They serve as a primary liaison between investigators, sponsors, and regulatory bodies to ensure study milestones are met.
11 days ago
University of California, Irvine
Coordinate and manage Phase I-IV cancer-related clinical trials, ensuring adherence to GCP, SOPs, and university policies. Act as a liaison between sponsors, regulatory agencies, and the research team while managing patient recruitment and data collection.
15 days ago
University of Massachusetts Medical School
The Clinical Research Coordinator manages human subject research protocols, including regulatory documentation, participant visits, and data collection. They ensure compliance with federal and institutional guidelines while supporting investigators with grant preparation and study reporting.
21 days ago
The Clinical Research Coordinator I manages regulatory activities, participant visits, and data collection for research protocols. They ensure compliance with IRB, HIPAA, and Good Clinical Practice guidelines while supporting the Principal Investigator.
23 days ago
The coordinator is responsible for managing human subject research, including regulatory activities, data collection, and participant coordination. Duties range from obtaining consent and tracking milestones to supervising staff and ensuring protocol compliance across multiple levels of seniority.
$40,000 - $80,000 / YEAR
24 days ago
KBR, Inc.
Educate military members and veterans on brain donation and manage the registration process for the Brain Donation Awareness Registry. Coordinate with medical examiners and funeral homes to recover, process, and ship brain specimens for CTE research.
25 days ago
Versiti, Inc.
Responsible for administrative tasks and clinical duties including phlebotomy, apheresis, and specimen processing for research studies. The role involves maintaining accurate data files, scheduling visits, and ensuring compliance with regulatory requirements.
29 days ago
Highmark Health
The role involves planning and managing clinical trials while ensuring compliance with regulatory bodies and human subject research standards. Key duties include identifying eligible patients, providing education to staff and participants, and maintaining clinical data and regulatory binders.
Coordinates all aspects of human subject research studies within the Cerebrovascular and Neurocognitive Research Group, including recruitment, enrollment, and study visit execution. Manages regulatory requirements, IRB submissions, and mentors junior research coordinators to ensure protocol compliance.
$25 - $35 / HOUR
1 month ago
Coordinates administrative and clinical activities for human subject research projects focusing on muscular dystrophy. Responsibilities include participant recruitment, regulatory document management, and overseeing data integrity for clinical trials.
Coordinates administrative and operational activities for human subject research, including participant recruitment, screening, and protocol adherence. Acts as a liaison between the Principal Investigator, sponsors, and the Institutional Review Board to ensure regulatory compliance and data accuracy.
Coordinates administrative activities for multi-site clinical research studies, including participant recruitment and consent. Manages study visits, ensures regulatory compliance, and assists in disseminating research findings through publications.
The Trainee will assist in the implementation of the ABCD Study by conducting neurocognitive tests, surveys, and biological sample collection. They are responsible for ensuring participant comfort, privacy, and adherence to IRB regulations and study protocols.
$19 - $26 / HOUR
Coordinates administrative and operational activities for human subject research, including participant recruitment, screening, and protocol adherence. Acts as a liaison between the Principal Investigator, sponsors, and regulatory bodies to ensure data accuracy and compliance.
General Dynamics Information Technology
The Clinical Research Assistant will recruit and screen study participants while performing data collection, scoring, and entry for clinical investigations. They will also maintain study documentation, ensure regulatory compliance, and assist with project improvement initiatives.
$21 - $24 / HOUR
UTHealth (University of Texas Health Science Center at Houston)
Coordinate day-to-day operations for clinical research studies, including participant recruitment, consenting, and visit scheduling. Manage data collection, regulatory submissions, and the preparation of research reports and grant proposals.
Coordinate and manage clinical trials in Movement Disorders, overseeing participant recruitment, data collection, and regulatory compliance. Serve as a liaison between investigators and sponsors while managing study documentation and reporting.
