* Maintained IT system -SIMS (Student Information Management System) * Maintained IT system - NC Wise for State of NC Department of Public Instruction * Performed activities for payroll, accounts payable and accounts receivable * Contract negotiation for all vendors as well as creating budget not only for vendors but for the Board of Directors as it pertained to the business of the school. * HR Manager Performed all HR functions * Member of policy committee for functions of all school programs and afterschool program. * Supervised office staff of four employees on a daily basis * Grant submission of after school program * Assisted with creating annual budget for school as well as after school programs. * Benefits Coordinator * Assisted with school audit by CPA firm as well as state audit by food and nutrition services. * Maintained all student files

* Responsible for day to day operations of development office * Managing a variety of projects as the general contractors/developers for the American Tobacco Project (200 million dollar project) * Performed activities for payroll, accounts payable, and accounts receivable * Executive Assistant to CEO, CFO, Development Director and Project Attorney * Developing the coordination of the ATC Art Project, which consisted of putting together the RFP and RFI? . * Setting panel committee for RFP review and overseeing the project from start to completing. * Community Development Coordinator * Submitting AIA Documents * Creating advanced power point presentations to be used in training by development, construction and legal departments.

Contract) Responsible for preparing study specific reporting forms and completes other required study set-up forms. Participates in clinical trial team meetings assigned trials/programs. Reviews protocol to ensure standard safety language is included and to identify any study specific safety reporting requirements. Participates where appropriate in CRA and Investigator Training including creation of slides and training materials. Assists in creating Safety Data Management Plans. Preforms reconciliation activities between clinical databases and safety databases. Identifies and prepares SAE case queries for assigned clinical trials in collaboration with Safety Physician. Participates in therapeutic area case management meetings for assigned clinical programs. Provides back-up support to the case handling group undertaking safety report intake, processing and reporting activities when required on an ad hoc basis. May also provide additional support to Sr. PV Ops Support Specialist for other development programs. Preparing CAPA reports for PVG risk management.

Short term contract -Responsible for the case processing of adverse event reports following company standard operating procedures, internal business practices and regulatory guidance documents, to ensure compliance with worldwide safety regulations and corporate policies.

Case prioritization based on seriousness of adverse events in accordance with SOPs (Standard Operating Procedures) and regulatory guidelines. Reviews medical record follow up to cases in litigation in accordance with US FDA Regulations. Analyzes and extract pertinent information from medical records in accordance with legal and US FDA safety regulations. Creates comprehensive narrative procured from relevant legal case documents and medical records as determined by regulatory and SOP guidelines. Data enters relevant information from completed extraction form from MRT or CRO (Clinical Research Organizations) into Argus LAM. Identifies and follow department procedures for AEs associated with product complaints.

Contract). Responsible for writing PVG SOP’s. Processing all AE/SAE and SUSAR cases for Medical Device Phase IV Post Marketing surveillance study. Responsible for preparing study specific study start up forms, as well as participating in all study start up kick off meetings. Preform monthly reconciliation activities between clinical databases and safety databases. Identifies and prepares SAE case queries for assigned clinical trials in collaboration with Safety Physician. Participates in therapeutic area case management meetings for assigned clinical programs. Participate in monthly signal detection meetings with PVG and Regulatory departments. Assist in the preparing of DSUR’s, PADER, and PSUR reports.

Safety Specialist at PPD