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. Provide safety monitoring for study participants. Carries out study-related activities under the supervision of local clinical management staff and in co-operation with Research Physician/(Associate) Medical Director. Reviews protocols for compliance with accepted research guidelines; 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; reporting adverse events in a timely manner, recording and entering data. In addition, assist with the guidance and supervision of staff in this role. May be expected to participate in team quality improvement efforts.
Duties of this position include following, in accordance with established policies and nursing standards:
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.