Clinical Research Coordinator managing the conduct of clinical trials at Emory University. Handling administrative activities and overseeing research project requirements and compliance.
About the role
- 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.
- Minimum of two (2) years of related experience
Benefits
- medical, dental and life insurance plans
- retirement plan options
- employee and dependent tuition programs
- generous leave
- hundreds of employee perks and discounts
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