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ICON plc
Overview
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance and data integrity while collaborating with investigators to maintain high-quality clinical data.
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Compensation
Salary not listed
Posted
17 days ago
The CRA is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They collaborate with investigators and perform data review to maintain high-quality clinical data for innovative treatments.
24 days ago
Emmes Group
The role involves supporting clinical research operations as an In-House CRA II. The position focuses on advancing medical discovery across various therapeutic areas including vaccines and rare diseases.
1 month ago
Fortrea
The role involves leading and supporting clinical trial monitoring activities, ensuring high standards of care for participants, and responding to emergencies based on clinical research standards. Responsibilities cover all aspects of study site monitoring, including routine monitoring, close-out visits, vendor liaison, and comprehensive site management as per project plans.
$105,000 - $117,000 / YEAR
ImmunityBio, Inc.
The Field Monitor will support clinical research teams by providing training, interpreting protocols, collecting and reviewing documents, and ensuring the efficient conduct of clinical studies. Key functions include developing training materials, serving as a Subject Matter Expert for sites, overseeing essential document collection, and managing investigational product supply.
$54 - $60 / HOUR
2 months ago
Responsibilities include leading and supporting the Full Service Outsourcing team by overseeing all aspects of study site monitoring, including routine monitoring, close-out visits, and maintenance of study files. The role also involves ensuring patient safety, adherence to protocol, data integrity verification via source document review, and managing Serious Adverse Event reporting.
$105,000 - $125,000 / YEAR
