Clinical Research Coordinator managing screening, enrollment, and retention of study participants for USF. Ensuring quality of data and implementing research procedures under supervision.
Responsibilities
Plans, organizes, and manages the resources necessary to achieve clinical research project goals and objectives at a single site.
Coordinates and performs patient clinical assessments for clinical trial visits for assigned clinical trial protocols including scheduling with vendors.
Communicates as a site representative with study sponsors, third party vendors, clinical teams and patients to ensure all protocol required elements are being completed and collected within the defined windows.
Ensures site compliance with research protocols, reviews case report forms and audits for accuracy with source documents.
Manages the site research project databases, develops flowsheets and other study related documents, and completes source documents/case report forms.
May provide guidance to other clinical research staff and support personnel.
Requirements
Bachelor's degree in a related field -OR- equivalent combination of education and experience.
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