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The Study Activation Coordinator is responsible for collecting study and site data feasibility, assessing institutional interest, and assisting in the determination of the appropriateness for CHC implementation. This position implements and manages study activation activities as applicable with study sponsors, CROs, and current CHC sites. This individual will work closely with the Director of Research Operations and other staff members to facilitate study selection and study activation activities supporting pharmaceutical, investigator initiated and consortia clinical trials. The Study Activation Coordinator reports directly to the Senior Director of Research Operations responsible for the study activation process.