Clinical Research Nurse
Job Family Early Development Services
PRA Location Lenexa, KS
Coordinate and participate in Phase I clinical research studies ensuring that studies are carried out according to protocol, standard operating procedures, and applicable guidelines and regulations. Review protocols for compliance with accepted research guidelines; submitting identifying, recruiting, and enrolling potential subjects after obtaining informed consent; ensuring adherence to written protocols including Health Insurance Portability and Accountability Act (HIPPA) regulations; collecting clinical data; performing phlebotomy and collecting other samples per research protocols; ensures appropriate laboratory, cardiopulmonary exercise tests and other diagnostic examinations are scheduled and completed per study protocols; communicates with study subjects regularly via follow-up visits and telephone contact; reporting adverse events in a timely manner, recording and entering data into a computerized database. In addition, assist with the guidance and supervision of staff in this role. May be expected to participate in team quality improvement efforts.
PRA is an Equal Employment Opportunity / Affirmative Action Employer
Nursing Degree and appropriate experience