Description
Roles:- Travels to field sites to monitor studies
- Collects and maintains legal and regulatory documentation, as applicable
- Ensures site compliance with regulations and study protocol
- Manages material logistics for the studies
- Works with Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
- Maintains a high level of professional expertise through familiarity with scientific literature, Company product portfolio, and competitve environments
Requirements:
- Bachelors degree in a scientific discipline or equivalent; MS or PhD preferred
- 6+ years of Clinical Research Associate experience
- Travel: up to 30%
- Medical device or diagnostic clinical trial experience
- Working knowledge of ICH GCP guidelines
To find out more about Real please visit www.realstaffing.com