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Responsibilities Travel to assigned research sites to manage day to day study operations including patient recruitment, screening, enrollment, and follow up visits Educate and support site personnel on study procedures, expectations, and compliance requirements Coordinate site opening activities to ensure new sites are prepared for study launch Support early enrollment efforts by guiding sites through startup tasks a
Competitive
Elite Clinical Network is seeking a Clinical Research Assistant to support the execution of clinical research studies under the supervision of the Clinical Research Coordinator and Principal Investigator. The role assists with participant coordination, data collection and entry, documentation, regulatory compliance, and study operations while supporting participant safety and adherence to Good Clinical Practice guide
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