Clinical Research Professional with 14+ years of experience in all aspects of managing Phase I-IV clinical trials encompassing pharmaceutical and medical devices. - Management of clinical trial site, which included, site selection and evaluation, trial set-up, study drug management (tracking, dispensing and disposal), investigator selection monitoring, regulatory submissions, trial reports and training of staff on clinical protocols. Proven successful management and leadership of multi-disciplinary teams in the planning, preparation and execution of clinical protocols. Consistently deliver high energy, dedication, enthusiasm, flexibility and adaptability in day-to-day project management responsibilities.