I have over sixteen (16) years of experience in Clinical Research Monitoring, including two (2) years as a Senior Clinical Lead in oncology. Also, prior experiences include site coordination, and nursing experience as an LPN with emphasis on Hematology/Oncology and Hospice care.I have extensive experience in implementation and monitoring of clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH guidelines. I also have skills in interpersonal communication, as well as establishing and maintaining rapport with health care providers and co-workers. I am organized, able to handle multiple tasks, work on deadlines and perform in high pressure situations.Specialties: My specialties includes emphasis in stage I-IV (PI initiated and pharmaceutical) studies in Oncology, Hematology, Gastroenterology, Neurology, Psychiatry, and Pulmonology.