Clinical Study Manager - (Plainfield, NJ)

Clinical Study Manager needs 4-five years relevant background Study Management Team Leader - Oncology is required with a BSc, three years with a MS/MPH, or 2 yrs with PharmD/PhD/MD Clinical Study Manager requires: Phase Ib/II/III Oncology trial background strongly preferred Global trial background strongly preferred Global Study Leadership of Pivotal NDA filing studies highly preferred PMP, CCRA certifications desired but not required. Background working in both sponsor and CRO organizations strongly preferred Background considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical device/Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization (CRO). CRA background is preferred. Time spent directly in a medical environment (e.g. as a Study Site Coordinator) is also considered relevan Clinical Study Manager duties: