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Children’s Hospital of Philadelphia
Overview
The coordinator will recruit and enroll participants for a longitudinal autism research study and manage study visits and biospecimen collection. They are also responsible for maintaining study source documents and ensuring adherence to IRB protocols and regulatory compliance.
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Compensation
$51,730 - $64,660 / YEAR
Posted
11 days ago
Children's Hospital of Philadelphia
The coordinator will recruit and enroll participants for a longitudinal autism research study and conduct study visits. They are responsible for managing study data, collecting biospecimens, and ensuring adherence to IRB protocols and regulatory compliance.
University of Rochester
Coordinate and oversee regulatory requirements for clinical research protocols, including documentation, filing, and tracking. Act as a liaison between study teams, sponsors, and regulatory committees to ensure compliance and study activation.
$51,810 - $72,534 / YEAR
17 days ago
Keck Medicine of USC
The Research Coordinator supports and coordinates daily clinical research activities in Cardiology, including recruitment, data collection, and IRB submissions. They work under the supervision of the Program Director and Principal Investigator to ensure compliance with federal and university regulations.
$32 - $35 / HOUR
18 days ago
Hospital for Special Surgery
Coordinates clinical research activities for the ARJR service, serving as a liaison between investigators, sponsors, and CROs. Manages all phases of study conduct, including recruitment, enrollment, regulatory compliance, and data maintenance.
Salary not listed
University of Southern California
The Research Coordinator supports daily clinical research activities in Cardiology, including recruitment, data collection, and IRB submissions. They collaborate with Principal Investigators to ensure studies are performed according to federal regulations and university policies.
Structure Therapeutics
The Senior Clinical Trial Associate serves as a central contact supporting the clinical study team in planning, implementing, and completing studies by interacting with sites, vendors, and team members. Key duties include obtaining, reviewing, and tracking study documents, setting up and maintaining the Trial Master File (TMF/eTMF), and facilitating meeting preparations.
$110,000 - $120,000 / YEAR
4 months ago
