Description
As a CRA you will be a part of a cutting edge study relating to Class III medical devices. You job duties and responsibilities will include but are not limited to; site monitoring, applying GCP to clinical trials, assemble and monitor site study binders, write site visit reports, interact with clinical professionals, clinical site visits, establish a clear understanding of project timelines and deliverables.Requirements:
BS degree or higher (RN is a plus)
3+ years CRA experience
Medical Device Experience
Ability to collaborate across teams
Vascular experience is a plus
This is a great opportunity to be a part of a cutting edge company and work on a challenging study. If interested please apply immediately.
To find out more about Real please visit www.realstaffing.com