Advanced Practice Provider - Research

Coordinate, implement, and complete clinical research studies by assisting with IRB submissions, recruiting participants, obtaining parental permission, and conducting study procedures. Provide specialty medical care, assessment, diagnosis, and management for patients enrolled in trials from 0 through 20 years, while performing clinical data gathering, monitoring data integrity, and maintaining study databases. Act as a patient advocate and liaison, evaluate treatment regimen compliance, and assist in reporting Serious Adverse Events. Schedule study visits, complete Case Report Forms, and coordinate monitoring activities with sponsor representatives. Mentor new clinical research coordinators and participate in training nursing staff for study purposes. Work Monday through Friday, 8:30 am to 5:00 pm, with no nights or weekends.