Description
Essential Functions:-Perform the activities associated with the implementation and monitoring of clinical trials.
-Oversee drug accountability at investigator sites and assist with the projection and management of both clinical and non-clinical supplies
-Assist in the preparation of clinical study reports, annual reports, IND updates, ect.
-Prepares and updates study drug forecasts.
-Work with Medical Monitor and CPM to select investigative sites, train investigators and investigate site staff, preparation o materials for investigator meetings, clinical supplies
-Provides training to internal and external customer needs
-Makes recommendation on appropriate study vendor(s) to Director or CPM and manages vendor to achieve project goals
-Contributes to wider organizational goals and activities as assigned
Requirements:
-BS/BA in a Science Field
-4+ years experience
-Phase III experience
-Oncology
-CRA background
To find out more about Real please visit www.realstaffing.com