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Fortrea
Overview
The role involves utilizing clinical skills and judgment to provide high standards of care in clinical research, including accurately performing vital signs, ECGs, collecting and processing biological samples, and monitoring participant compliance with meals.
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Compensation
Salary not listed
Posted
1 month ago
CenExel
The role involves executing laboratory procedures according to protocol, assisting the laboratory manager with site preparation, and maintaining detailed logs for sample handling and inventory. Responsibilities also include obtaining, processing, and properly storing biological samples while ensuring equipment and storage temperatures are maintained.
$20 - $21 / HOUR
2 months ago
Benaroya Research Institute
The core responsibilities involve coordinating and conducting clinical research study visits, including participant recruitment, informed consent, data collection, and ensuring compliance with study protocols and regulations. This role supports translational research focused on immune-mediated diseases within the Center for Interventional Immunology.
$26 - $45 / HOUR
The Clinical Research Nurse will utilize their skills and judgment to provide a high standard of care in clinical research, which includes performing vital signs, venipuncture, ECGs, processing biological samples, and monitoring participant meals for compliance. Key duties also involve assisting with room preparation, medical equipment setup, and screening procedures while maintaining a safe working environment.
3 months ago
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for CRFs.
The coordinator ensures the highest standards of data quality and participant safety are maintained, along with adherence to protocols, SOPs, and regulatory guidelines. This involves assisting the QA Manager, reviewing various monitoring reports and logs for trends, and performing ongoing quality reviews of study documentation.
The coordinator is responsible for managing all phases of clinical trials from initiation to completion, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. This includes organizing research information, monitoring subjects, performing safety assessments, and handling administrative and regulatory duties.
5 months ago
