Experienced Clinical Research Coordinator III (Regulatory) with 13 years in Oncology Clinical Trials. Serving as a liaison between the industry, sponsor, investigators, and the IRB.Responsible for managing multiple Oncology Cooperative Group Clinical Trials such as NRG, SWOG, ECOG, and NCI.Responsible for managing 45 plus Oncology Clinical Trials with various cohorts and phases.Submits new studies, annual reviews, adverse events, SAEs, outside safety reports, study amendments for Oncology Clinical Trials to the IRB.I have had 1 Coorperative Group and 3 Clinical Trials audited by the FDA with no regulatory findings.Demonstrated history of working in the hospital & health care industry.Skilled in Microsoft Office, Word, and PowerPoint, excellent communication skills, consistently achieves set objectives, detailed oriented, self motivated, team player.Strong research professional with a Bachelor's of Science degree in Nursing.