The Research Study Coordinator works under the general direction of the Principal Investigator to assist with the coordination of protocol implementation for multiple research studies. The Research Coordinator performs, as delegated, the day-to-day activities for multiple studies with respect to compliance, regulatory, recruitment, initiation, monitoring and close out throughout the course of the research trials. The coordinator follows protocol, institutional and regulatory requirements to assure accuracy of the study procedures being conducted.
EDUCATION: * High School Diploma or GED (Required)
2 year / Associate's Degree in Health Sciences or related field (Preferred)
4 year / Bachelor’s Degree in Health Sciences or related field (Preferred)
Combination of relevant education and experience may be considered in lieu of degree.
CERTIFICATION/ LICENSURE/ REGISTRATION:
Certification as a Clinical Research Associate through ACRP or SOCRA
EXPERIENCE AND SKILLS:
*1-2 years experience as a research coordinator (Required)
Advanced Microsoft Office skills – including Word, Excel and PowerPoint
*2 - 4 years Proven ability to use independent judgment and function autonomously (Required)
2 - 4 years Working knowledge of medical terminology (Preferred)
Working knowledge of research regulatory and compliance