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UPMC
Overview
Coordinate oncology-focused clinical trials by managing patient recruitment, informed consent, and data collection. Collaborate with multidisciplinary teams to ensure protocol compliance and protect patient safety and rights.
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Compensation
Salary not listed
Posted
22 days ago
West Virginia University
The Clinical Research Specialist will coordinate and implement operational tasks for neuromodulation brain therapeutics research projects. Responsibilities include ensuring protocol compliance, managing patient care, facilitating informed consent, and maintaining accurate research documentation.
1 month ago
K2 Staffing LLC
The Quality Control Associate monitors and performs routine compliance checks on all source data according to protocol requirements and regulatory standards like ICH-GCP and FDA Regulations. Key duties include reviewing source documents for eligibility verification, confirming adherence to organizational policies, and serving as a quality point of contact for sites.
5 months ago
