Description
Roles:- Reviews study protocols, reports and manuscripts
- Travels to field sites to monitor studies
- Collects and maintains legal and regulatory documents
- Manages material logistics for the studies
- Manages training and coordinating certification of study site personnel
- Ensures accurate and complete study management/ data collection
Requirements:
- Bachelors degree in a scientific discipline
- Experience with diagnostic or medical device clinical trials
- Familiar with EDC systems
- Scientific laboratory or molecular PCR experience
- Experience with source data monitoring in a field monitoring environment
- 3-5 years of previous experience as a CRA in the industry
- TRAVEL: up to 30 % during occasional peak periods
To find out more about Real please visit www.realstaffing.com