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Emory University
Overview
The Clinical Research Coordinator II manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, ensuring protocol compliance, and supervising specimen collection.
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Compensation
Salary not listed
Posted
14 days ago
The coordinator manages administrative activities for clinical trials, including data entry, patient recruitment, and specimen collection. They are also responsible for maintaining equipment, tracking regulatory submissions, and coordinating study procedures.
The coordinator manages administrative activities for clinical trials, including database management, participant recruitment, and consenting. They ensure protocol compliance, prepare regulatory submissions, and oversee the collection and processing of study specimens.
17 days ago
The coordinator manages administrative activities for clinical trials, including database management, participant recruitment, and ensuring protocol compliance. They are also responsible for processing study specimens and preparing regulatory submissions.
21 days ago
The Clinical Research Coordinator II manages administrative activities for clinical trials, including database management and regulatory submissions. They are responsible for recruiting and consenting participants, supervising specimen collection, and ensuring strict protocol compliance.
25 days ago
Ochsner Health
This role manages and executes clinical trial activities, including patient recruitment, screening, and the administration of investigational therapies. The researcher serves as a liaison between patients and principal investigators while ensuring strict adherence to Good Clinical Practice guidelines.
26 days ago
1 month ago
The Clinical Research Coordinator II manages research project databases, develops study-related documentation, and ensures compliance with research protocols. They also interface with research participants to determine eligibility, obtain consent, and coordinate study procedures.
The Clinical Research Coordinator assists with the administrative conduct of clinical trials, including data management, patient recruitment, and medical record reviews. They also perform clinical tasks such as phlebotomy and specimen processing while ensuring regulatory compliance.
The Clinical Research Coordinator II manages research project databases, develops study documents, and ensures compliance with research protocols. They also interface with participants to determine eligibility, obtain consent, and coordinate study procedures.
2 months ago
The Clinical Research Coordinator manages administrative activities for clinical trials, including data entry, patient recruitment, and maintaining study documentation. They also perform clinical tasks such as specimen collection, phlebotomy, and monitoring regulatory submissions.
The Clinical Research Coordinator II manages research project databases, develops study-related documents, and ensures compliance with research protocols. They also interface with participants to determine eligibility, obtain consent, and supervise the collection and processing of study specimens.
