The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials. The position requires data management, patient recruitment, and quality assurance. Additional responsibilities include equipment maintenance, medical record review, and specimen collection.
Requirements
- Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
- Assists with patient recruitment.
- Orders and maintains equipment and supplies.
- Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
- Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
- Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
- Assists with quality assurance and tracks regulatory submissions.
Benefits
- Emory University offers a comprehensive benefits package, including medical, dental, and vision insurance, retirement savings, paid time off, and more.
- Emory University is committed to providing equal opportunities for all employees.
- Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request.