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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.
Perform hands-on practical and administrative activities for early phase clinical trials, including phlebotomy and vital signs monitoring. Responsible for collecting biological samples and ensuring dietary compliance for research participants.
11 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, 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
ICON plc
The Clinical Research Nurse executes Phase 1 clinical trials by performing core nursing tasks such as IVs, EKGs, and blood draws. They are responsible for documenting assessments and adverse events while ensuring adherence to ICH-GCP and study protocols.
18 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.
Coordinate and execute the screening and eligibility determination of volunteers for early phase clinical trials. This includes conducting clinical tasks like vitals and ECGs, obtaining informed consent, and maintaining participant data in databases.
24 days ago
IQVIA
The IDS Pharmacist ensures protocol integrity, patient safety, and regulatory compliance for Phase 1 Oncology trials. Responsibilities include medication dispensing, compounding, inventory management, and supervising IDS technicians.
$57,700 - $209,800 / YEAR
25 days ago
Hackensack Meridian Health
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials, ensuring compliant patient care and regulatory adherence. Responsibilities include recruiting patients, managing informed consent, monitoring patient progress, and acting as a liaison between investigators and sponsors.
$55,962 / YEAR
29 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 Clinical Research Nurse I will utilize their skills and clinical judgment to provide a high standard of care in clinical research, ensuring participant dignity, health, safety, and welfare are the highest priority. Key duties include responding to emergencies, administering investigational compounds, performing study-related activities like cannulation and ECGs, and managing the Informed Consent process.
2 months ago
