The primary purpose of the Clinical Studies Coordinator is to provide clinical evaluation, coordination, implementation, and monitoring of patients enrolled in phase I research protocols. Also serves as an effective point of contact regarding status and progress of phase I trials. Impacts clinical trials patients in designated protocols. Utilizes medical or clinical knowledge for supervised non-clinical patient interaction for the purposes of research data gathering and monitoring. Requires strict adherence to the policies and procedures of the institution.
The ideal candidate will have experience in clinical trial and/or health research and demonstrate the ability to effectively multi-task while maintaining exceptional organization and attention to detail. Familiarity with Epic and/or OnCore is desirable. The candidate should be proficient in Microsoft Excel, PowerPoint, and Word, and possess strong analytical and communication skills. An advanced degree is preferred
Minimum $27...