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Mount Sinai Health System
Overview
The coordinator is responsible for conducting clinical research studies, obtaining informed consent, and organizing study information. They also assist in the preparation and submission of grant applications and IRB documents.
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Compensation
$17 - $41 / HOUR
Posted
7 days ago
Vanderbilt University Medical Center
The Research Nurse Specialist 2 maintains the integrity and quality of clinical research trials, planning recruitment, managing enrollment, and ensuring protocol compliance under occasional guidance. Key duties include preparing research proposals, performing administrative tasks, utilizing nursing skills for procedures, and observing/reporting adverse events.
Salary not listed
10 days ago
American Addiction Centers
The Research Fellow will implement community-based human subjects research studies and manage the collection and analysis of quantitative and qualitative data. They will also engage with community partners and produce high-quality scholarly writing, including manuscripts and grant applications.
$31 - $46 / HOUR
17 days ago
Johns Hopkins University
Coordinate clinical trials and research projects for the Multiple Sclerosis and Stiff Person Syndrome Centers. Responsibilities include participant recruitment, consenting, data collection, and managing regulatory paperwork and IRB submissions.
$17 - $30 / HOUR
23 days ago
University of Massachusetts Medical School
The Clinical Research Coordinator II will coordinate regulatory activities and manage data collection for complex research protocols. They will also ensure compliance with study protocols and assist with participant interactions and documentation.
$48,000 - $55,000
Oregon Health & Science University
The Senior Clinical Research Assistant manages patients on clinical trials, including consenting, enrolling, and gathering data. They are also responsible for regulatory tasks, sample processing, and assisting the Clinical Research Manager with various projects.
$48,734 - $77,522 / YEAR
24 days ago
UCSF
Execute and coordinate clinical research protocols, including data collection and the management of human biospecimens. Manage regulatory documents, IRB submissions, and ensure compliance with institutional and agency policies.
$32 / HOUR
25 days ago
NCIRE - The Northern California Institute for Research and Education, Inc.
The incumbent will serve as a Study Coordinator providing day-to-day coordination for several research studies focused on women's health and sleep. Key tasks include participant recruitment, conducting assessments, and managing study documentation and data.
$25 - $41 / HOUR
1 month ago
The Research Program Coordinator develops and participates in study protocols, designs management and statistical plans, and analyzes data. They are responsible for conducting human subjects or laboratory research and preparing final study reports.
$58,661 - $81,675 / YEAR
The coordinator administratively manages clinical protocol implementation, ensuring adherence to study guidelines and validity of findings. Responsibilities include participant recruitment, consenting, data collection, and the processing and tracking of biospecimens.
The coordinator conducts and assists in clinical research studies under the supervision of senior staff. Key duties include obtaining informed consent, organizing study information, and assisting with grant and IRB submissions.
University of New Mexico
Support medical research studies in an emergency care setting by screening participants and obtaining informed consent. Collect research data from patients and medical records while handling biological specimens according to protocols.
$17 / HOUR
Medical University of South Carolina
Perform complex laboratory tests and molecular procedures to support clinical trials, including sample procurement, processing, and shipping. Maintain accurate data records and ensure compliance with regulatory standards and laboratory safety protocols.
$52,100 - $88,600 / YEAR
Heluna Health
The Research Coordinator manages day-to-day operations for a NIDA-funded study, including participant recruitment, consent, and data collection. They serve as the primary liaison between the Syringe Services Program and the Lead Study Team to ensure protocol compliance.
The coordinator will administratively manage clinical protocol implementation and ensure the logistical execution of study activities. Key duties include participant recruitment, consenting, data collection, and coordinating submissions to the Institutional Review Board.
The coordinator administratively manages clinical protocol implementation for neurology studies, ensuring adherence to protocols and validity of findings. Key duties include participant recruitment, consenting, data collection, and coordinating with the Institutional Review Board.
The coordinator conducts and assists in clinical research studies under the supervision of a Principal Investigator. Key duties include obtaining informed consent, organizing study information, and assisting with grant and IRB submissions.
The Clinical Research Coordinator assists lab leadership in conducting clinical research studies. Responsibilities include managing human subjects research and ensuring adherence to study protocols.
NYU Langone Health
The Research Coordinator manages the coordination of research studies, including participant recruitment, enrollment, and data collection. They ensure protocol execution follows Good Clinical Practices and HIPAA regulations while interfacing with patients and principal investigators.
$66,300 - $68,250 / YEAR
