Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
University of Rochester
Overview
This role coordinates human subject research activities within the Department of Urology, focusing on screening, consenting subjects, maintaining documentation, and managing data collection according to research protocols. The specialist ensures research activities adhere to institutional policies, IRB requirements, and study protocols while coordinating with the Principal Investigator and other study team members.
Quick view →
Compensation
$21 - $30 / HOUR
Posted
8 days ago
Sanford Health
Organize and coordinate complex components of clinical trials, including patient recruitment, screening, and the administration of investigational treatments. Maintain accurate study documentation, resolve data queries, and collaborate with physician investigators to ensure protocol compliance.
$24 - $39 / HOUR
23 days ago
UCSF
The role involves supporting daily clinical trial operations with a primary focus on study data entry and coordination. Responsibilities include recruiting subjects, managing study documentation, and ensuring the collection and shipment of samples.
$32 - $39 / HOUR
1 month ago
The role involves supporting clinical trials primarily through study data entry and the coordination of active or follow-up trials. Responsibilities include recruiting subjects, gathering medical data, and preparing reports and protocols under the supervision of a manager.
$32 - $38 / HOUR
The incumbent will perform entry-level duties to support and coordinate clinical studies for participants with language difficulties at the UCSF Memory and Aging Center. Responsibilities include recruiting and scheduling subjects, managing study data, preparing protocols, and assisting with clinical trial documentation.
$38 - $61 / HOUR
2 months ago
K2 Staffing LLC
The Quality Control Associate monitors and performs routine compliance checks on all source data according to protocol requirements and regulatory standards like ICH-GCP and FDA Regulations. Key duties include reviewing source documents for eligibility verification, confirming adherence to organizational policies, and serving as a quality point of contact for sites.
Salary not listed
5 months ago
