Overnight RN

Overnight RN-Research Nurse

• Research Nurse is responsible for study unit activities in the conduct of Phase 1 clinical trials with emphasis on the safety and welfare of study participants

• Enroll patients into clinical trials: Informed Consent (ICF) process- educating, explaining and informing participants of study procedures

• Utilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials

• Utilize nursing assessment skills to observe participant general well-being and potential adverse events.

• Document adverse events and take appropriate action as needed

• Obtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study procedures

• Perform study-related activities such as Cannulation, telemetry, holters, vital signs, ECGs, venipuncture

• Collect and processes biological samples according to the protocol and Standard Operating Procedures

• Record data obtained in a timely, error free manner according to the protocol and Standard Operating Procedures

• Transcribe source data onto the Case Report Form

Qualifications

• RN License must be active and in good standing in Wisconsin

• Associates Degree

• Nursing experience in a patient facing setting

• CPR and ACLS Certifications