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Care Access
Overview
The coordinator is responsible for screening, enrolling, and monitoring clinical research subjects while ensuring strict adherence to protocols and regulatory guidelines. Key duties include performing clinical procedures, managing study documentation, and coordinating with sponsors and investigators.
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Compensation
$60,000 - $90,000 / YEAR
Posted
24 days ago
Oregon Health & Science University
The role supports clinical trial operations by assisting with patient visits, data collection, and regulatory documentation for cardiovascular research. Key duties include scheduling participants, coordinating travel, and ensuring data entry into central repositories meets sponsor timelines.
$48,734 - $77,522 / YEAR
1 month ago
Benaroya Research Institute
The role provides administrative and clinical support for cancer clinical research, including managing regulatory documents and scheduling participants. Clinical duties involve performing blood draws, EKGs, and processing biological samples.
$23 - $31 / HOUR
Medpace, Inc.
The Project Coordinator will engage in clinical trial management and work closely with the project CTM to ensure timely delivery of tasks. Responsibilities also include compiling project status reports, interacting with sponsors and study sites, and managing study supplies.
Salary not listed
The role involves engaging in day-to-day clinical trial management, working closely with the CTM to ensure timely and accurate task delivery. Responsibilities also include compiling status reports, interacting with various stakeholders, and managing internal regulatory filing oversight and study supplies.
The intern will provide day-to-day project support activities, including maintenance of project-related files and correspondence with study teams. Additional tasks include coordinating meetings, maintaining databases, and managing study supplies.
2 months ago
