Description
An all round Clinical Research Associate needed. Someone who has multiple therapeutic area experience and multiple Phase experience I-IV.As a Senior CRA you will be responsible for:
- Site management and site staff performance including monitoring all types of clinical trials ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
- Data Handling, Reporting and Tracking & administrative tasks
- Perform management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines.
- May assume the role of a Lead CRA (LCRA) on projects by providing direction and guidance to project team, coordinating all monitoring activities, and communicating the status of these activities to the study Project Leader
We are seeking candidates with the following key attributes:
- Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
- Extensive clinical monitoring experience
- Experience or education indicates a sound basic knowledge of medical and pharmaceutical terminology
- Extensive understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines
KEYWORDS: CRA, SCRA, CLINICAL RESEARCH ASSOCIATE, SPAIN, PHASE I-IV, CNS
To find out more about Real please visit www.realstaffing.com