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Essen Medical Associates
Overview
The Limited Permit Provider collaborates with the care team to assess and coordinate chronic disease management for patients. They are responsible for conducting comprehensive evaluations, managing medical conditions, and ensuring effective discharge planning under the supervision of licensed providers.
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Compensation
$50,000 - $70,000 / YEAR
Posted
1 month ago
Revival Research Institute, LLC
The Clinical Research Coordinator will manage multiple studies, including participant screening, recruitment, and enrollment. They are also responsible for collecting and processing research specimens, maintaining source documents, and assisting with regulatory document preparation.
Salary not listed
Coordinate and manage multiple clinical studies while assisting principal investigators with participant screening, recruitment, and enrollment. Maintain accurate study documentation, handle data queries, and ensure compliance with regulatory standards and quality control methods.
Coordinate and manage multiple clinical studies while assisting Principal Investigators with participant screening, recruitment, and enrollment. Maintain accurate study documentation, handle data queries, and ensure compliance with quality control and regulatory standards.
Coordinate and manage multiple clinical studies while assisting principal investigators with participant screening, recruitment, and enrollment. Maintain accurate study documentation, process research specimens, and ensure compliance with regulatory standards and quality control methods.
The Clinical Research Coordinator will manage multiple studies, assist Principal Investigators with participant recruitment, and handle data collection and specimen processing. They are also responsible for maintaining trial documentation, ensuring quality control, and communicating with study sponsors and the Institutional Review Board.
The Clinical Research Coordinator will manage multiple studies, including participant screening, recruitment, and enrollment. They are also responsible for collecting and processing research specimens, maintaining trial documentation, and assisting with regulatory document preparation.
The role involves coordinating and managing multiple clinical studies, assisting Principal Investigators and clinical staff with study-related tasks. Responsibilities include participant screening, data collection, document maintenance, and communication with study sponsors.
5 months ago
