Research Nurse II

JOB REQUIREMENTS: Position Description: Purpose To provide safe and
effective nursing services, document complex research observations, and
perform precise collection of research data and specimens per protocol
to ensure quality control and assurance in clinical research. Primary
Functions Perform basic or complex nursing services as defined in the
Wisconsin Nurse Practice Act. Maintain nursing licensure and ensure all
certifications (CITI/BLS), nursing competencies, and assigned
MCW/Froedtert training modules and vaccinations are completed on time.
Assure compliance with all relevant Internal Review Boards (IRB) and
other regulatory requirements, including proper protocol documentation,
verifying informed consent, and maintaining the confidentiality of
participants and research data. Assist in the collection and evaluation
of data and specimen – Including vital signs/ECGs
reports/saliva/sweat/blood/urine. Administer protocol specific
interventions up to and including infusions, transfusions, injections,
vaccinations, oral medications, vascular access (IV/Port/PICC),
spirometry testing, survey collection, and venipuncture phlebotomy.
Assist study teams with safe transfers and lift services to control the
risk of injury to participants and research staff. Educate and empower
participants/coordinators/peers with strategies and best practices to
improve health and research outcomes. Facilitate unit workflow by
assisting with scheduling, visit assignments, chart preparation,
protocol translation, study specific training, and general study
coordination, Provide excellent customer service and support to all ATRU
users, including principal investigators, study coordinators,
participants, pharmacy, and other research personnel. Coordinate the
development, implementation, and monitoring of Quality Improvement
activities for the unit. Implement and conduct quality control processes
to ensure the highest data standards. Identify problems or obstacles in
the system/procedures related to implementation of the research
protocols, data collection, and communicate to the study investigators.
Notify appropriate personnel of any complications or untoward effects of
research, including adverse reactions and/or protocol deviations. Work
closely with leadership to maintain compliance and process improvement.
Perform additional tasks as assigned. Consider the participant safety
and ethical concerns by verifying informed consent,
identifying/reporting adverse events, advocating for the participant,
and complying with the Health Insurance Portability and Accountability
Act (HIPAA). Communicate in a language that will resonate… For full
info follow application link. EEO/AA Minorities/Females/Vets/Disability
The Medical College of Wisconsin is an affirmative action/equal
opportunity employer and does not discriminate in hiring or employment
on the basis of age, sex, race, color, religion, national origin,
veteran status, disability or sexual orientation. APPLICATION
INSTRUCTIONS: Apply Online: ipc.us/t/6BE5A79221C343D2 Qualified females,
minorities, and special disabled veterans and other veterans are
encouraged to apply.