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University of Virginia
Overview
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.
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Compensation
Salary not listed
Posted
14 days ago
Beth Israel Lahey Health
The Clinical Research Coordinator is responsible for the coordination and administration of multiple research studies, including implementing protocols and managing study progress. They facilitate clinical trials by screening and recruiting participants while collecting and reporting accurate study data.
$19 - $31 / HOUR
1 month ago
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
The Clinical Research Coordinator I will coordinate and administer multiple research studies, working closely with principal investigators and research staff. Responsibilities include implementing study protocols, managing study progress, and interacting with study participants.
Physician Affiliate Group of New York
The Clinical Research Coordinator executes clinical trials by managing day-to-day operations, ensuring strict protocol adherence, and safeguarding participant well-being through procedures like ECGs and phlebotomy. This role involves directing participant screening, enrollment, managing the informed consent process, and closely monitoring patients for adverse events.
$70,000 / YEAR
Wayne State University
The coordinator will coordinate and participate in clinical research studies by performing data collection and compilation, working with principal investigators to execute various study tasks efficiently. Essential duties include recruiting, screening, obtaining informed consent, scheduling visits, interacting with subjects, and accurately recording study data.
$56,131 - $67,354 / YEAR
PIH Health
The Clinical Research Coordinator manages and coordinates clinical research studies within a hospital, ensuring adherence to regulatory requirements and institutional policies. This role supports the day-to-day execution of clinical trials through participant recruitment, data collection, compliance monitoring, and regulatory documentation.
$27 - $45 / HOUR
INSIGHT Surgical Hospital
The Clinical Research Coordinator will support principal investigators, act as a liaison between sponsors and the institute, and oversee the details of clinical studies, ensuring compliance with review boards and regulations across multiple research projects. Key duties include providing technical support, directing trial operations, managing enrolled patients, maintaining regulatory documents, and reporting adverse events to all governing bodies.
3 months ago
University of Texas Medical Branch (UTMB)
This role involves conducting a variety of non-routine research assignments and experiments, specifically assisting Principal Investigators in the Department of Obstetrics and Gynecology with research duties. Key tasks include protocol development related to imaging components of sheep studies and assisting with the acquisition and analysis of images from in vivo studies.
$20 / HOUR
University of Chicago
This role involves performing routine assignments for scientific research projects, ensuring compliance with all regulatory policies, and assisting in complex laboratory duties such as planning, execution, and organization of research activities. Responsibilities also include data collection, analysis, literature reviews, and contributing to the writing of academic papers and reports.
$24 - $34 / HOUR
Astera
The Clinical Research Coordinator will provide overall coordination for study-related activities for patients in cancer research studies, ensuring activities adhere to local and federal regulations and sponsor policies. Responsibilities include assisting with IRB submissions, maintaining regulatory documents, coordinating patient tests and visits, and entering research data into a centralized database.
NCIRE - The Northern California Institute for Research and Education, Inc.
The incumbent will conduct structured clinical interviews and neuropsychological testing for multiple PTSD-focused research studies, including administering measures like SCID and CAPS to determine eligibility and collect post-intervention data. Responsibilities also involve scoring tests, entering data into databases, advising on participant eligibility, maintaining documentation, and participating in data analysis and report preparation.
$48 - $74 / HOUR
4 months ago
The University of Toledo
This role leads monitoring regulations and guidance to ensure the implementation of changes to operational processes or best practices for clinical research. The specialist provides expert advice to investigators and personnel on ensuring compliance throughout the lifecycle of clinical research and trials.
5 months ago
