Description
Essential Functions and Duties:- Demonstrates a strong working knowledge of clinical research processes, Good Clinical Practices, International Committee on Harmonization Guidelines, federal regulations and applicable local laws pertaining to clinical research investigations. Working knowledge of ICH-GCP/ISO14155 and relevant SOPs, as required
- 3 or more years of monitoring experience
- Computer literacy, proficiency in MS Office
- Excellent interpersonal and organizational skills and attention to detail
- Oncology experience preferred
Requirements:
- Bachelor's degree in scientific discipline or applicable
- 3+ years experience as a CRA in biotech or pharma
- Strong proficiency in GCP and ICH guidelines
***Additional details upon request
To find out more about Real please visit www.realstaffing.com