Description
Roles and Responsibilities:- Independent and proactive coordination of all necessary activities required to set up and monitor a study (i.e., identify investigators; help prepare regulatory submissions, conduct pre-study and initiation visits, etc.).
- Approximately 50-70% travel overall can be expected, national and regional travel.
- Demonstrate product and procedure knowledge to support study-related questions and provide site training.
Requirements:
- 4-6 years of clinical monitoring experience
- 4 year degree in a science related field
- Experience with oncology, neurology, or cardiovascular
- Regional monitoring experience in past is a huge plus
To find out more about Real please visit www.realstaffing.com