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4 C Medical Technologies
Overview
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
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Compensation
$75,000 - $95,000 / YEAR
Posted
6 days ago
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
9 days ago
Best Care
Coordinates clinical research studies including regulatory compliance, study start-up, subject follow-up, and record maintenance. Manages trial oversight, participant safety, and the handling of investigational products.
Salary not listed
28 days ago
Nationwide Children's Hospital
Manages clinical study elements including recruitment, enrollment, and day-to-day management following ICH/GCP guidelines. Responsible for collecting research data, processing human specimens, and maintaining regulatory binders.
29 days ago
1 month ago
Forward Health LLC
The Clinical Research Coordinator manages and executes clinical trials at the site level, ensuring compliance with study protocols and regulatory guidelines. They serve as the primary liaison between the Principal Investigator, study participants, and sponsors while overseeing subject recruitment, data management, and safety monitoring.
$17 - $35 / HOUR
K2 Staffing LLC
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and ongoing reporting. They also collaborate with clinical operations, sponsors, and IRBs to ensure audit-ready regulatory files and compliance with study protocols.
2 months ago
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and close-out procedures. They also collaborate with clinical operations and sponsors to ensure audit-ready regulatory files and compliance with protocol requirements.
University of Colorado
The Regulatory Affairs Coordinator independently manages all IRB and regulatory processes for ophthalmology research studies. Responsibilities include preparing regulatory submissions, maintaining investigator site files, and ensuring compliance with institutional and federal regulations.
$59,995 - $87,761 / YEAR
