Dedicated to Merck Oncology's Global Clinical Operations as a Global Trial Optimization Specialist.

• Prepares and submits all materials for the Institutional Review Board (IRB) and otherRegulatory bodies as required by the protocol to ensure compliance in a timely fashion.• Performs regular quality control assessments to ensure that clinical trial data is collectedand stored per GCP.• Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).

Review regulatory documentation submitted from domestic and international research sites participating in National Cancer Institute sponsored NCTN designed clinical trials.Analyze IRB documentation for compliance with federal code (21 CFR 50 45 CFR 46) to ensure strict adherence and to prevent ineligible enrollment of patients. Provide regulatory support to research associates and physicians globally with regard to the integration of Lead Protocol Organizations RTOG/NRG, COG, SWOG, Alliance, and ECOG-ACRIN; Federal agencies NCI CIRB, CTEP, PMB, and FDA; NCI Contracted agencies CTSU, Westat, and RSS.Organize team meetings to enhance client relations and cross-team efficiencies.

Under the Municipal Court, I met with the Public one on one to convey requirements for filing Small Claims cases up to $10,000 and Landlord Tenant actions. Within the Criminal Justice center, I facilitated enrollment of parties into Private Criminal Complaint Arbitration hearings by describing the process and options available.