UTS Temporary Clinical Research Coordinator at UNC Chapel Hill

Position Summary
The Research Assistant is responsible for supporting the lead coordinators in coordinating multiple complex trials through the protocol life cycles of activation implementation and closure. Research Study Execution * Collect study data through a variety of methods per study protocol (e.g. administer surveys observe/conduct study activities and record outcomes electronic medical record data abstraction biospecimens). * Perform clinical tests and procedures in accordance with the study protocol following adequate training. * Record and organize study data and complete applicable case report forms (electronic or paper) as required in accordance with good clinical practice and ALCOA -C principles. * Manage study visits as applicable (e.g. schedule/coordinate visits prepare materials manage research charges etc.) Research- Subjects/Ethics * Maintain administrative study documentation (e.g. delegation of authority logs training records) * Assist in the development and submission of regulatory applications and/or study materials (e.g. recruitment materials informed consent forms) * Gather and store required regulatory documentation. * Prepare for study monitoring participate in monitoring visits and assist with corrections as applicable. * Track and document protocol deviations and adverse events. Participant Management * Screen and recruit study participants for studies per study protocol and applicable standard operating procedures. * Obtain informed consent from study participants. Research- Project Management * Participate in basic study start-up activities. * Participate in site initiation visits study start-up meetings and closeout visits for research studies. Research- Quality Control * Ensure accuracy of data collected by conducting quality assurance/quality control procedures. * Report variations or discrepancies in data collected. Recognize discrepancies in patterns and make recommendations for process improvement. Research- Lab Operations * Maintain study supplies (e.g. laboratory kits administrative supplies). * Track and ship biospecimens as applicable.

Preferred Qualifications Competencies And Experience
Experience in clinical research EPIC medical records experience

Work Schedule
Monday Friday 8am 5pm Onsite

Required Experience:

Staff IC