Top Global CRO looking for an RN
The 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
RN or LPN in good standing in the state of Wisconsin.
On-site in Madison, WI.
If interested please call 309-661-4927 or email email@example.com
This post was authored by Kelli Richards on 05/31/2023.