The UNC Kidney Center is seeking a full-time, temporary Research Coordinator to assist in the implementation of clinical research studies being done with adults and children with kidney disease. Responsibilities will include: preparation and submission of the initial regulatory packets for clinical trials, both sponsored and PI initiated; submission, organization and maintenance of all IRB documents associated with the clinical studies; maintenance of regulatory binders for studies; the evaluation and recruitment of potential subjects for study participation; preparation for study visits of the patients and per protocol ordering of lab and diagnostic procedures; performance of clinical procedures and assessment of study subjects while obtaining study information and specimens (blood and urine); specimen processing and shipping; data collection and entry into computerized data capture systems or transcribing data onto case report forms; responding to data queries and coordinating study monitoring visits.
The individual in this position must be able to multi-task effectively and attention to detail is paramount, for this person will be responsible for the coordination and management of numerous regulatory and reporting requirements for multiple clinical research projects. Knowledge of ICH GCP guidelines is essential.
Education and Experience
Bachelor’s degree in a relevant field or equivalent combination of training and experience. Must have basic knowledge of Microsoft Office Products including Word and Excel.
Special Physical and Mental Requirements
Temporary Employment Policies
University of North Carolina at Chapel Hill - 23 months ago