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Quality Systems RN And Research Coordinator Full Time Days
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Full-time
- The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct of all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Clinical Research Manager and affiliated Director.
- The CRC provides operational support in the management of patients accrued to multiple research protocols to assure subjects’ safety and regulatory compliance.
- The CRC is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, Standard Operating Procedures and all applicable regulations and guidelines and ensuring effective data flow associated with research protocols.
- Preferred: Two to three years of experience in Clinical Research to include healthcare compliance, research auditing, monitoring standards, or related experience.
- Preferred field of expertise: Research, Performance Improvement, Utilization Management, Risk Management and Infection Control
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