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Mass General Brigham
Overview
The coordinator assists with clinical research studies by recruiting and consenting patients, collecting data, and performing clinical tests. They are also responsible for scheduling protocol-mandated tests and ensuring compliance with regulatory requirements.
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Compensation
$29 / HOUR
Posted
2 days ago
University of Miami
The Clinical Research Coordinator 2 assists in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies, managing day-to-day operations from initiation to close-out according to regulatory guidelines. This role involves ensuring participant safety, adhering to approved protocols, handling administrative tasks, facilitating information flow, and coordinating study activities and personnel.
Salary not listed
12 days ago
The Clinical Research Coordinator 2 manages the day-to-day operations of clinical research protocols from initiation to close-out. Key duties include participant recruitment, data collection, specimen processing, and ensuring adherence to regulatory and sponsor guidelines.
Provides assistance on clinical research studies by recruiting and consenting patients and collecting study data. Performs clinical tests such as phlebotomy and EKGs while maintaining regulatory binders and documentation.
17 days ago
University of Rochester
This role involves assisting in the planning, coordination, implementation, monitoring, and evaluation of assigned clinical research studies, ensuring adherence to regulatory guidelines from initiation to close-out. Key functions include coordinating participant enrollment, managing study documentation, performing data entry and quality checks, and maintaining study continuity for moderate-sized studies.
$25 - $35 / HOUR
3 months ago
University Hospitals
The role involves providing safe, age-specific nursing care to patients while coordinating and implementing assigned clinical research studies according to Good Clinical Practice guidelines. Responsibilities include managing regulatory documentation submissions, recruiting participants, obtaining informed consent, conducting nursing assessments, and maintaining accurate study records.
