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University of Virginia
Overview
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.
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Compensation
Salary not listed
Posted
2 days ago
University of Iowa
Manage and support clinical trial regulatory activities for the Pediatric Department, including IRB submissions and documentation. Act as a back-up study coordinator to assist with subject visits, data entry, and protocol execution.
3 days ago
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.
Duke Careers
This role involves managing all aspects of clinical research operations within the Anesthesiology Clinical Research Unit, including preparing FDA regulatory submissions, managing investigational products, and ensuring protocol compliance across various settings.
$59,829 - $99,960 / YEAR
12 days ago
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.
13 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 Research Nurse Coordinator I manages complex research protocols, ensuring adherence to GCP standards and regulatory requirements. They act as a primary liaison between clinical partners, investigators, and sponsors while overseeing patient care and data integrity.
21 days ago
University of Rochester
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
Mount Sinai Health System
The coordinator assists in daily clinical research activities, including obtaining informed consent and organizing study information. They also help prepare grant applications and documents for the Institutional Review Board and Grants and Contracts Office.
UCSF
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
University of Oklahoma
Coordinate multiple cancer outcomes research protocols, including participant enrollment and data management using REDCap and OnCore. Collaborate with principal investigators and the IRB to develop protocols and contribute to manuscript development.
Johns Hopkins University
The specialist manages regulatory maintenance for oncology clinical trials, including IRB submissions and internal quality control. They also support program operations, train research staff, and facilitate compliance with institutional and federal research guidelines.
$48,000 - $84,100 / YEAR
The Assistant Clinical Research Coordinator supports cancer-related clinical trials by managing data, coordinating protocol requirements, and assisting the Principal Investigator with patient recruitment and screening. They also serve as a liaison between sponsors, regulatory agencies, and the research team to ensure compliance with institutional and federal policies.
The role involves planning, coordinating, and implementing clinical research studies while ensuring adherence to regulatory guidelines and protocol standards. Responsibilities include managing participant enrollment, maintaining research records, and performing quality checks to ensure data accuracy and participant safety.
The Clinical Research Coordinator will independently execute and manage research protocols for pediatric oncology and hematology studies. Responsibilities include overseeing data integrity, maintaining regulatory documents, and coordinating study operations across multiple departments.
$38 - $42 / HOUR
The specialist is responsible for the coordination and oversight of regulatory requirements for clinical research protocols. They manage documentation, maintain logs in tracking systems, and act as a liaison between study teams, sponsors, and regulatory committees.
This role involves coordinating and implementing clinical trial research studies, working closely with Principal Investigators on all assigned projects, which includes managing recruitment, obtaining informed consent, and overseeing ongoing study conduct activities. Responsibilities also cover preparing and submitting all necessary regulatory documentation to the IRB, managing study billing reconciliation, and ensuring effective communication with study Sponsors.
2 months ago
Coordinates and implements clinical trial research studies within the Department of Plastic Surgery, working closely with Principal Investigators. Responsibilities include managing IRB protocols, patient recruitment, data collection, and regulatory documentation.
The Clinical Research Coordinator will independently execute, manage, and coordinate research protocols for pediatric oncology and hematology studies. They are responsible for overseeing study operations, data collection, and ensuring compliance with institutional and regulatory policies.
