Clinical Research Assistant

Great benefits including 401k w/match and 15 days PTO Monday-Friday, 8:30 AM - 5 PM Great opportunity to get involved in clinical research! About Our Client Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors. Responsibilities Assist in coordinating the research trial process with CRCs, Site Managers, and PIs Assists in educating patients about the nature of the trials and the benefits and risks of participating Determine protocol-related needs to conduct the trial and order supplies and equipment Recruits and screens potential patients and obtains informed consent Completed source documents and forms to facilitate accurate data collection and record keeping Conducts in-service programs and summarizes study schedules to assist in understanding and implementing a protocol Schedules patient visits and laboratory and diagnostic test procedures Assists with investigational product shipments, storage, and accountability Review trends, problems encountered, patient adverse events, and patient progress Perform other clinical skills as required by the trial protocol, including vital signs, ECGs and blood glucose testing Qualifications 1+ years of experience in a medical setting, working with patients. Bachelor's degree preferred Phlebotomy and EKG experience preferred Familiar with using electronic platforms for medical data #J-18808-Ljbffr