Detailed-oriented, highly-motivated Clinical Research Professional with both pharmaceutical and CRO project management experience in various therapeutic areas. Effectively manage startup, maintenance, and close-out activities of multiple Phase I-IV, multicenter, US and global clinical trials on time, within scope, and compliant with study protocols, FDA guidelines, GCPs and SOPs. Provide administrative and research support and leading activities related to development and execution of cross-functional and 3rd-party deliverables.