Dedicated Clinical Research Professional with more than 15 years of experience. Broad background in Pharmaceutical Enterprise and biotech clinical trials management of phases II/III/IV trials in therapeutic areas which include dermatology, genitourinary, nephrology, urology, prostate cancer, infectious disease, orthopedics and obstetrics and gynecology to include study start-up activities, implementation of study protocols, on-site data management (collection and monitoring), quality assurance and study closeout. Experience with USA and Canada regulations.