 Member of the Executive Management team with global responsibility for operation teams including Project Management, Project Setup Management, Investigator Services, Specimen Management, Logistics and Kit Packing (150+ Global team members) Responsible for the development, management and adherence to departmental budgets Work with Executive Management to devise strategies for operational delivery Develop and maintain key client relationships and ensure optimal service level across operations Aligns with Leadership team to problem solve and evaluate internal processes in support of key performance indicators

 Manage all aspects of Project Management, Project Setup Management and Investigator Services Responsible for all key deliverables, personnel and processes in each functional area Participate in key client meetings Overall responsibility for instigating and leading change initiatives within the department Serves as a liaison with Business Development and Bids/Contracts for the client presentations and proposal development

 Works across multiple divisions to direct the delivery of projects within cost, time and quality requirements Consults with leadership in all functional areas on the continuous development/improvement of business processes to support cross functional teams and to ensure that work is uniform, complete and managed appropriately Assists in resource utilization, policy development, and implementation of goals Directs through lower management levels and / or highly skilled specialist employees who exercise significant latitude and independent judgment

 Responsible for the overall coordination and management of clinical trials teams and studies from start up through close out Direct technical and operational aspects of the project to ensure compliance with FDA regulations and PPD procedures Work across functional areas to identify and evaluate any issues, interpret data and implement solutions in order to ensure successful completion of trials Oversee project specific training for project team members Analyze costs, personnel hours and project needs to determine the most cost effective and efficient means to ensure that all project deliverables meet the client’s needs and adhere to the contract

 Overall responsibility for the quality management system Assures all necessary policies and procedures are in place and followed in order to comply with all government,ISO9001, and customer requirements Continuously monitors and improves the performance of the quality system Assures project management gathers all required information in order to communicate customer requirements to theinternal team Overall responsibility for the quality management system Assures all necessary policies and procedures are in place and followed in order to comply with all government,ISO9001, and customer requirements Continuously monitors and improves the performance of the quality system Assures project management gathers all required information in order to communicate customer requirements to theinternal team Develops quality programs, documented processes and procedures in order to assure proper execution of projects

 Oversee all functions of Study Support Operations including Project Setup, Investigator Services and Kits and Logistics Review clinical protocols and mentor staff regarding key deliverables Establish and ensure standardization of procedures and efficiencies within Clinical Trial Division and across globalplatform Develop, monitor, forecast department operating budget, labor supply and utilization Oversee resource allocation and project financials Represent Clinical Trials at regulatory, client interactions and at audits Support sales and marketing initiatives.

 Directs and supervises the daily activities of project team members to initiate new clinical trial protocols and supportexisting business in accordance with customer requirements Monitors, trains, and advises staff. Communicates with customers to negotiate and document project scope andrequirements Develop standard operating procedures Participates in interview and selection of new hires

 Review clinical protocols and assist with protocol set-up functions Develops protocol specification documents along with investigator manuals and protocol specific operatingprocedures Performs basic monitoring function for applicable protocols Compiles project metrics and analyses all activity related to the trial Prepares and conducts investigator training. Performs troubleshooting and problem solving functions throughout the study.

 Supported clinical protocols that included various types of image analysis included CAT Scan, Magnetic ResonanceImaging etc. Primary contact for imaging activities throughout the Iife cycle of the project Responsible for overall study delivery