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Fortrea
Overview
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management for oncology clinical trials. Ensures data integrity, patient protection, and adherence to protocol and regulatory requirements.
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Compensation
$115,000 - $140,000 / YEAR
Posted
1 month ago
Responsible for all aspects of clinical site monitoring, including routine visits, close-outs, and site management. Ensures patient protection, data integrity, and adherence to study protocols and regulatory requirements.
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 Telemetry Technician will provide continuous cardiac monitoring and clinical support for research participants in Phase I clinical trials. Responsibilities include interpreting telemetry data, performing ECGs, documenting vital signs, and ensuring study protocol compliance.
Salary not listed
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
