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Iterative Health
Overview
The intern assists Clinical Research Coordinators with the conduct of research studies, focusing on patient eligibility and recruitment. Key tasks include reviewing protocols, screening subjects, and documenting patient information in clinical management systems.
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Compensation
Salary not listed
Posted
2 days ago
Fresenius Medical Care
Provides administrative and clinical support for clinical trials, including the collection of regulatory documents and performance of study-specific procedures. Assists with subject screening, informed consent, and accurate data entry into case report forms under the supervision of the Principal Investigator.
3 days ago
University of Florida
Collaborate with research staff and physicians to ensure protocol compliance and patient care for cancer research trials. Responsibilities include transcribing clinical data, coordinating sample collection, and facilitating regulatory documentation for the IRB.
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The Clinical Research Assistant will assist in managing multiple clinical trials, ensuring compliance with protocols and regulations. Responsibilities include data entry, patient recruitment, and performing phlebotomy and ECGs.
5 months ago
