Clinical Research Nurse II Per Diem Night

Work Schedule
Other

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Reviews inclusion/exclusion criteria with patients to ensure eligibility to

participate in study. Interacts with Principal Investigator for inclusion/exclusion

review of patient data. Reviews and witnesses the consenting process for

subjects. Prepares study-specific documents for applicable study visit.

• Ensures the safety of patients by monitoring and assessing AEs, if any, and

communicating potentially serious findings to investigators.

• Performs all procedures in the treatment areas (i.e., check-ins, gauze

management, administration of drug, blood draws, ECGs, vital signs, etc.).

Monitors staff to assure adherence to GCP, ICH, FDA, and OSHA guidelines.

• Attends initiation meetings when necessary to obtain study process clarification.

• Monitors and continuously evaluates the overall research experience of each

patient to assure a positive experience.

• Performs other study-related duties as qualified by documented training.