Katie Flaherty Email and Phone Number

· Responsible for the efficient management of our property services. Services include collecting monthly rent, security deposit and return, lease drafting and full execution, initial walkthrough, vacancy and annual inspections, coordinating maintenance requirements and selection of tenants through the screening process.· Responsible for file management of HUD listings from intake to final sale. Includes uploading of information thru designated management system, accurate and complete file organization, timely correspondence with HUD management company and provide excellent customer service to potential buyers.· Ensures the smooth and efficient day to day operation of the office; acting as the primary point for questions regarding the offices' services.

Ensures the smooth and efficient day-to-day operations of the clinical research center for a multi-specialty health care organization.Manages the contracting, budgeting and regulatory aspect of clinical trails. Responsible for the development, implantation and adherence to standard operating procedures.Proficient in industry guidelines i.e. ICH, GCP, FDA Code of Federal Regulations.Responsible for the development, tracking and compliance of meeting department metrics in relationship to safety, quality, excellence and financial goals.

· Collaborated closely with the Research Manager and Director of Research to review and negotiate Clinical Trial Agreements and evaluate the costs of potential studies. Negotiated study costs with the sponsor in an accurate and timely fashion.· Maintained accurate tracking of patient visits, stipends, invoices, and sponsor reimbursement.· Maintained site compliance with the Food and Drug Administration (FDA) regulations that govern performance of clinical studies· Responsible for accurate regulatory submissions to Institutional Review Boards (IRBs), sponsors, and CROs in a timely manner· Maintained organized and accurate site regulatory files.· Responsible for close collaboration with the sponsor and FDA during regulatory inspections

· Proficient in reviewing clinical information with research patients including medical history, medications, vital signs, and symptoms while documenting the data in adherence with the protocol.· Responsible for identifying potential research patients through rigorous chart review and adherence to protocol inclusion/exclusion criteria.· Maintained organized screening records, screening logs, and screening database for the research department.· Processed and shipped laboratory specimens in accordance with IATA/IACO certification.· Proficient in developing source documentation and maintenance.· Responsible for accurate regulatory submissions to Institutional Review Boards (IRBs), sponsors, and CROs in a timely manner.· Maintained organized and accurate site regulatory files.