Successfully managing several clinical trial protocols simultaneously. Ensuring that they met all regulatory and FDA compliance initiatives (GCP, GLP, CFR Part 11 and HIPPA).Project set up of multiple studies at the same time, all setup was in place by the first patient visit. Forecasting project revenue to ensure deliverables are met. Writing policies and procedures to ensure regulatory practices are met. Data locks on time with all deliverables met for client submission. Protocol training and training document construction at the request of the client. Technical consultations as requested by the sponsor in regards to protocol set up. Experience in all therapeutic area clinical trials. Source document creation and database management. Managing data coordination using MS Access for data analysis.Ensure the team meets all agreed-upon deadlines, follow procedures, collaborate with colleagues, and follow through on project requirements and deliverables. Trained, supervised and evaluated staff, coached improvement management skills. Successfully refined and implemented new procedures for department training. Training of associates and support staff to ensure quality and customer service. Redefined goals and objectives for support staff and project associates. Reviewing and updating staff policies and procedures to ensure all activities are cost efficient. Mentoring staff for company driven promotions.Specialties: Knowledge of Oncology clinical trialKnowledge of laboratory processProject ManagementKnowledge of FDA compliance initiatives (GCP, GLP, CFR Part 11 and HIPPA).Time managementBudget and forecastingProcess improvement and SOP developmentTesting and validation of systemsWriting training programs