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Charlotte, NC, United States
Job ID: 137820
Job Family: Research Services
Status: Full Time
Shift: Day
Job Type: Regular
Department Name: 55541005040306-Vaccine Trials
Overview
Job Summary
Manages protocols to ensure the safety of patients and quality of clinical trial data. Prepares and submits Institutional Review Board (IRB) paperwork and maintains all related regulatory document submissions. Communicates and coordinates study activities with the Primary Investigator and any Sub-Investigators of clinical studies.
Essential Functions
Physical Requirements
Works in clinical care areas and office environments. May be required to travel. Requires close, personal contact with patients, handling of blood and body fluids, walking, sitting, standing, lifting, handling of charts, supplies and equipment, and operation of a keyboard and computer. Responsibility to work in a safe manner.
Education, Experience and Certifications
Bachelor’s Degree and research experience required. Master’s Degree preferred. Phlebotomy certification or venipuncture skills preferred. BLS HCP certification from AHA preferred. Certification in clinical research (SoCRA, ACRP) preferred.