Description
Summary:The Clinical Research Associate (CRA) will assist with the implementation of multiple clinical research projects.Responsibilities:
- Clinical site selection, study initiation visits, training of on-site personnel, study close-out visists
- Assist with vendor and CRO management, clinical budget allocation, and on-site monitoring
- Responsible for timely identification of problems or issues that could affect the results or timely completion of the trial, or any protocol deviations, and for suggesting mechanisms for solving the problem.
- EDC and TMF - data management and analysis
Requirements:
- BS, RN, BSN preferred; or degree equivalent
- Experienced with In Vitro Diagnostic (IVD) products
- Working knowledge of ICH GCP guidelines and FDA regulations
- 2+ of prior monitoring experience in industry
- Knowledgeable in field of oncology and infectious disease
- Lab or science research experience strongly preferred
- TRAVEL: 40-50%
To find out more about Real please visit www.realstaffing.com