Description
Essential Responsibilities:- Independently manage the study start up activities for a multi-center, US based IVD study
- Responsible for clinical site training and adherence of the site to protocol, according to ICH/GCP guidelines, regulations, and SOPs
- Mentor and coach junior staff (CTAs)
- Conduct study qualification visits for the purpose of assessing the site's ability to effectively conduct the trial per SOP and study guidelines
- Perform relationship management tasks and evaluate CRO performance
Requirements:
- RN background is strongly preferred; will consider BS/BA in scientific discipline
- 5+ years of clinical trial monitoring experience
- OB or diagnostic experience is preferred
- At least 5 years of medical device clinical trial experience
- TRAVEL: 40-50 %
To find out more about Real please visit www.realstaffing.com