Clinical Research Coordinator - Research SUMMARY: CRC monitors and coordinates multiple research projects in order to assess the need for and to implement strategies to ensure the conduct of quality research, the achievement of expected timelines and deliverables, and the efficient use of resources. CRC is responsible for assisting PIs with study protocol development, ICFs, and required study documents in preparation for IRB submission. Assists with recruitment activities, consents patients, ensures eligibility prior to enrollment, and randomizes patients to study. Abstracts data, completes case report forms and maintains research record and data integrity. Schedules and meets with study monitor for site visits, maintains data in an audit ready state, and ensu
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