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Fortrea
Overview
Perform clinical tasks including venipuncture, ECGs, and vital signs readings for healthy volunteers in Phase 1 clinical trials. Collect and process biological samples according to study protocols while maintaining a safe and efficient clinic environment.
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Compensation
Salary not listed
Posted
5 days ago
The role is responsible for the operational conduct of assigned clinical studies, ensuring compliance with regulatory requirements and protocols. Key duties include study set-up, coordinating critical events, monitoring participant safety, and facilitating study planning meetings.
10 days ago
The role is responsible for the operational conduct of assigned clinical studies, ensuring compliance with regulatory requirements and protocols. Key duties include study set-up, coordinating critical events, and managing participant safety and eligibility.
Provide high-standard clinical care to healthy volunteers in Phase 1 clinical trials, ensuring participant safety and welfare. Responsibilities include administering investigational compounds, performing clinical procedures, and documenting adverse events according to study protocols.
12 days ago
Perform clinical tasks including venipuncture, ECGs, and vital signs monitoring for healthy volunteers in Phase 1 clinical trials. Ensure strict adherence to study protocols and maintain a clean, safe clinical environment.
16 days ago
Provide high-standard clinical care to healthy volunteers in Phase 1 clinical trials, ensuring participant safety and welfare. Responsibilities include administering investigational compounds, performing clinical procedures like venipuncture and ECGs, and documenting adverse events.
18 days ago
The Paramedic will provide high-standard clinical care by collecting blood samples, performing vital sign checks, and monitoring study participants during Phase 1 clinical trials. They are also responsible for accurately recording research data, maintaining medical equipment, and ensuring participant safety and protocol compliance.
1 month ago
The Research Nurse will provide high-quality clinical care to participants in early-phase clinical trials while ensuring protocol compliance and participant safety. Responsibilities include performing study-related procedures, monitoring for adverse events, and maintaining accurate documentation in an electronic environment.
2 months ago
