What are the responsibilities and job description for the Clinical Research Nurse II Per Diem Night position at Thermo Fisher Scientific?
Work Schedule
OtherEnvironmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety StandardsJob 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.
