Clinical Research Nurse working for the Clinical Trials Unit (CTU) with patients in clinical research studies.
Screen, obtain consent and follow subjects for clinical research studies.
Enroll subjects in studies and schedule follow-up visits.
Work with clinical investigators and staff to manage research subject profiles including screening, assessing and monitoring study medications.
Will need to know/learn how to pack and ship biological samples.
Must be able to draw blood, obtain vital signs, and do EKG’s.
Need to be flexible to work clinic hours as needed.
(A) Education requirement:
Some college desirable
(B) Licenses or certifications:
LPN or RN; Certified Clinical Research Coordinator by ACRP.
(C) Technical/computer skills:
MS Word; Excel; Red Cap, data base and study data entry; sponsor reporting.
(D) Prior experience:
At least 1-year applicable experience.