medical community networking or internal BMS requests, to assist in the placement of planned clinical studies with qualified... activities through frequent visits and contacts to monitor study sites following the monitoring plan and applicable BMS SOPs...
authority submissions and obtain IRB/regulatory approvals for conducting the clinical trial. Assist PM in start-up meetings.... Participate in investigator meetings as necessary. Prepare and manage the clinical trial agreements with investigators/sites...
area and is responsible for developing and executing the late development (Phase II – III) clinical strategies and plans... o Experience publishing results of a clinical trial in a peer-reviewed journal is required o Extensive pharma/biotech industry...