Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Fortrea
Overview
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.
Quick view →
Compensation
Salary not listed
Posted
10 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
$113,610 / YEAR
1 month 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.
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