Registered Nurse-Clinical Research
Schedule: Rotating shifts (1st, 2nd, 3rd) + every other weekend

+ 1st Shift: 5:00 AM – 7:00 AM start

+ 2nd Shift: 2:00 PM – 4:00 PM start

+ 3rd Shift: 10:00 PM – 12:00 AM start

+ Schedules are finalized 2–3 weeks in advance

Key Responsibilities

+ Conduct study unit activities in support of Phase 1 clinical trials

+ Ensure the safety, rights, and well-being of all study participants

+ Facilitate and continuously support the Informed Consent (ICF) process, providing clear education on study procedures

+ Enroll participants into clinical trials and guide them throughout the study

+ Perform clinical assessments to monitor participant health and identify adverse events

+ Accurately document adverse events and escalate appropriately

+ Perform study-related procedures, including:


+ Cannulation

+ Venipuncture

+ Vita...