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IQVIA
Overview
The intern supports the preparation, documentation, and management of investigational products for clinical trials under pharmacist supervision. Key duties include managing drug accountability logs, dispensing medications per protocol, and ensuring regulatory compliance with FDA and IRB standards.
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Compensation
$33,000 - $82,600 / YEAR
Posted
2 days ago
Hackensack Meridian Health
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials, ensuring compliant patient care and regulatory adherence. Responsibilities include recruiting patients, managing informed consent, monitoring patient progress, and acting as a liaison between investigators and sponsors.
$55,962 / YEAR
28 days ago
University of Rochester
Coordinates administrative and operational activities for human subject research, including participant recruitment, screening, and protocol adherence. Acts as a liaison between the Principal Investigator, sponsors, and the Institutional Review Board to ensure regulatory compliance and data accuracy.
$21 - $30 / HOUR
1 month ago
Coordinates administrative activities for multi-site clinical research studies, including participant recruitment and consent. Manages study visits, ensures regulatory compliance, and assists in disseminating research findings through publications.
Coordinates administrative and operational activities for human subject research, including participant recruitment, screening, and protocol adherence. Acts as a liaison between the Principal Investigator, sponsors, and regulatory bodies to ensure data accuracy and compliance.
Beth Israel Lahey Health
The Clinical Research Coordinator manages the administration of multiple research studies, ensuring protocol adherence and regulatory compliance. Key duties include recruiting and screening participants, collecting study data, and maintaining communication with sponsors and investigators.
$19 - $31 / HOUR
$113,610 / YEAR
Wayne State University
The coordinator will coordinate and participate in clinical research studies by performing data collection and compilation, working with principal investigators to execute various study tasks efficiently. Essential duties include recruiting, screening, obtaining informed consent, scheduling visits, interacting with subjects, and accurately recording study data.
$56,131 - $67,354 / YEAR
2 months ago
Emory University
The Clinical Research Coordinator II manages administrative aspects of clinical trials, including maintaining databases, completing source documents, and providing guidance to junior staff. This role involves interfacing directly with research participants for eligibility determination and consent, as well as ensuring strict compliance with research protocols.
Salary not listed
3 months ago
