Possesses knowledge and understanding of policies, procedures, and regulations governing human subject's research and
incorporation of them in the conduct of research and care of participants.
Proficiently prepares and processes new research proposals, amendments, continuing review applications and adverse
events.
Perform administrative duties for trials, including but not limited to: Procuring equipment, preparing documentation, and
packaging and shipping medications.
Utilize nursing skills to perform procedures, deliver individualized care, and abide by research protocols. If problems arise,
identify and implement solutions, assuring goals are met.
Performs the procedures required of each study protocol, understanding standard of care versus research. Continually
assesses the need for additional protections for research participants.
Recruit and identify the eligibility of candidates, regularly assessing them to ensure continued eligibility for participation.
Troubleshoots trial recruitment strategies to ensure trials are completed in a timely manner.
Provides education and training to appropriate personnel and participants in research specific methodology and
procedures.
Utilizes knowledge of disease processes to observe for and report adverse events to the principal investigator and all
regulatory authorities as required by protocol, policies and procedures and regulations.
The responsibilities listed are a general overview of the position and additional duties may be assigned
1+ years of Oncology bedside nursing, Infusion nursing, travel nursing, ICU nursing, or ER nursing.
Active RN license in State of TN
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.