Job Description
Overview
- $20 - $22/hr
- 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 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