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Medpace, Inc.
Overview
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.
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Compensation
Salary not listed
Posted
1 month ago
JENAVALVE TECHNOLOGY INC
The Senior Clinical Research Associate will support the conduct of pre-market clinical studies, ensuring compliance with regulatory requirements, and will manage data collection, query resolution, and status reporting for clinical staff and management. Responsibilities also include conducting EDC training, maintaining Trial Master Files, managing regulatory documents, and supporting clinical audits.
$95,000 / YEAR
2 months ago
The Clinical Research Associate will proactively support the conduct of pre-market and/or post-market clinical studies, ensuring compliance with all regulatory requirements under the Director of Clinical Affairs. Key duties include supporting site management, ensuring quality data management, maintaining trial documentation, and conducting internal file audits for compliance.
$75,000 / YEAR
Bellefaire JCB
The specialist will monitor clients' emotional conditions and facilitate daily care by providing emotional support, assistance, and motivation while working alongside licensed professionals. Responsibilities also include participating in progress evaluation, facilitating treatment programs on various topics, and protecting clients from harm using the Therapeutic Crisis Model of Intervention.
$19 / HOUR
3 months ago
