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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
Mass General Brigham
This role supports research studies in Sleep and Circadian Disorders by instructing subjects, obtaining informed consent, collecting, organizing, and analyzing study data, and preparing regulatory documentation. Responsibilities also include creating REDCap surveys and databases, training personnel, and troubleshooting specialized data collection devices during various shifts.
$20 - $29 / HOUR
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
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
UTHealth Houston
Identify and recruit participants for cancer screening and HPV vaccination programs within the greater Houston area. Deliver educational sessions and provide follow-up health coaching and navigation to help participants overcome barriers to care.
10 days ago
Nevada System of Higher Education
The Research Coordinator will support the Stress, Pregnancy, & Health (SPAH) Kids study by managing IRB documentation, recruiting participants, and administering cognitive and psychosocial assessments. Additionally, the role involves data management, assisting with manuscript preparation, and coordinating grant-related activities.
$25 - $37 / HOUR
Coordinate data collection and operations for the SNAK clinical trial, focusing on participant recruitment, enrollment, and retention. Manage study data, administer surveys, and connect families to community-based resources under the supervision of the Primary Investigator.
11 days ago
Duke Careers
The specialist will support clinical research operations by managing participant documentation, data collection, and regulatory compliance for cancer studies. They will also collaborate with investigators to facilitate participant recruitment, study visits, and the preparation of research materials.
$21 - $31 / HOUR
13 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.
$59,829 - $99,960 / YEAR
The Lab Specialist will provide technical lab support by performing high-quality lab and research tasks, including processing bio-specimens, managing clinical databases, and assisting with research evaluation. Key duties involve recruiting, screening, and enrolling study participants, collecting data via interviews, obtaining informed consent, and coordinating sample collection from clinics.
New York State Psychiatry Institute
The Research Coordinator will assist with study implementation, regulatory management, and participant coordination. They will oversee daily trial operations and ensure protocol adherence.
$46,021 - $54,975 / YEAR
24 days ago
University of Miami
The Clinical Research Support Specialist assists in the recruitment, screening, and enrollment of study participants while managing data collection and regulatory documentation. They also conduct community outreach, schedule research visits, and maintain consistent communication with participants to ensure study adherence.
Coordinates clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. Responsible for maintaining regulatory binders, performing data analysis, and assisting the Principal Investigator with reports and presentations.
$24 - $39 / HOUR
28 days ago
Washington University in St. Louis
Assists the Principal Investigator in coordinating clinical research studies, ensuring regulatory compliance and IRB support. Manages project infrastructure, including budget oversight, data management via REDCap, and participant coordination.
$23 - $34 / HOUR
29 days ago
The Co-op Assistant supports clinical research studies by developing patient recruitment strategies and managing data collection. They are also responsible for processing blood samples, maintaining regulatory binders, and performing administrative scheduling tasks.
$18 - $24 / HOUR
NCIRE - The Northern California Institute for Research and Education, Inc.
Coordinate and manage clinical trials focusing on PTSD, TBI, and sleep disorders, combining research tasks with administrative operations. Responsibilities include collecting psychophysiological data, managing regulatory documents, and overseeing participant recruitment and scheduling.
$25 - $41 / HOUR
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.
1 month ago
Mount Sinai Health System
Participate in clinical and translational research focused on Parkinson's disease and other neurodegenerative disorders. Duties include processing brain tissue, performing histology, writing autopsy reports, and managing the brain donation process.
UCSF
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.
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.
