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Cooper University Hospital
Overview
Assists the Principal Investigator with IRB protocols, consent forms, and study budget development. Responsible for recruiting study participants and maintaining all required study documentation for the IRB and FDA.
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Compensation
$23 - $37 / HOUR
Posted
2 days ago
Theradex Oncology
The Clinical Research Associate will conduct site monitoring visits, including qualification, initiation, routine, and close-out visits to ensure protocol compliance and data integrity. They will also act as a liaison between study sites and the project team while managing site documentation and safety reporting.
$75,000 - $145,000 / YEAR
1 month ago
Fortrea
The CRA will lead and support the Medical Device & Diagnostics team by managing all aspects of study site monitoring, including routine visits and close-outs. They are responsible for ensuring protocol adherence, data integrity, and the protection of study participants through rigorous clinical research standards.
$105,000 - $117,000 / YEAR
The CRA 2 is responsible for all aspects of study site monitoring, including routine visits, site management, and maintenance of study files. They ensure protocol adherence, data integrity, and the protection of study participants while managing serious adverse event reporting.
The CRA is responsible for all aspects of study site monitoring, including routine visits, site management, and ensuring protocol adherence. They also manage data integrity, handle serious adverse event reporting, and coordinate clinical projects as a local contact.
$105,000 - $145,000 / YEAR
2 months ago
