Description
Duties:- Design and develop clinical protocols.
- Design case report forms.
- Manage vendors required to conduct clinical studies.
- Oversee performance of CROs and field CRAs
- Prepare required documentation from clinical sites prior to study start-up
- Participates in clinical data review.
- Maintains accurate clinical study documentation.
Requirements:
- 5 years vendor management experience
- 10 years industry experience
- BS/BA required
- Effective communication skills
- 25-30 percent travel
To find out more about Real please visit www.realstaffing.com