Clinical Studies Management

Clinical Studies Managers across clinical disciplines will support our clinical/physician principal investigators in managing and coordinating clinical studies where they may not have the trained personnel to support clinical research needs. The services offered are to assist in assessing study feasibility and reviewing the protocol and pricing, assist with IRB preparation, manage communications between departments and sponsors, handle site preparation, recruitment and informed consent, study visits, study conduct and completing case report forms, managing source documents and test articles, adverse event management, and study close out.

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