I am an experienced clinical research professional with over 15 in the pharmaceutical industry working on the Vendor, CRO and large and mid size pharmaceutical and biotechnological companies. As an experienced Global Senior Clinical Trial Manager, with oversight of clinical operations in North America, Latin America, Europe, and Asia Pacific (including Australia), I have managed large high-profile Phase III programs.I have successfully delivered on milestones throughout all stages of trial management, from site identification and selection, to final database lock and close-out activities. I have experience in all aspects of clinical trial operations (including Protocol/ICF Development, Study Management, Clinical Team Management, Monitoring, SOP Development/Implementation, Training, Budget Management), FDA Regulations, and ICH/GCP Guidelines.I have experience in Phase 1, Phase II, Phase Ila, Phase Ill, and Phase IV studies, including pediatric and adolescent populations. My therapeutic experience includes Hematology Oncology, Cardiovascular, Urology, Respiratory and Women’s Health. I consistently demonstrate strong skills in leadership, teamwork, and attention to detail (frequently receiving recognition from client team members, as well as internal functional leads). I am a self-motivated, results-oriented individual and my core competencies include client communications, timeline review, GCP compliance, budget management, resource management, and staff training/ supervision. I possess excellent computer, communication, writing, and organizational skills.