➢ Lead, Development of Educational materials for National and Regional thought leaders➢ Lead, Development of Educational Curricula for physicians and extended care givers and for National Health Systems➢ Presentation of Clinical and Scientific data at key National Academic and Managed Care accounts➢ Developed Educational materials (disease states, anatomy, pathophysiology) for National and Regional sales forces➢ Faculty Member, Merck Academy➢ Lead, Medical Assistant University Education Development Project➢ Six Sigma Development and Implementation Team for Regional Medical Director Program, External Medical and Scientific Affairs➢ Scientific Liaison and Communication for Merck & Co., Inc., EMSA (External Medical and Scientific Affairs) representing Clinical Research Division, Outcomes Research Division, Medical Services and Academic and Professional Affairs➢ Review and evaluation of Merck Foundation and Investigator Scientific Collaboration and Research Grants➢ Representative of Merck & Co., Inc. on key scientific committees➢ Served as a medical consultant to Regional Executive Management teams, Specialty and Sales teams, Hospital and Managed Care teams➢ Identification and coordination of clinical research sites ➢ Member, Cardiovascular Scientific Advisory Team - Heart Failure and Hypertension➢ Core member, Strategic, Business and Marketing teams➢ Scientific Liaison Officer for National Cross Functional Teams➢ Merck Award for Excellence (2/2014) – commitment to building talent on Health Systems team, driving results, and fostering collaboration ➢ Merck Special Achievement Awards (3/2008), (7/2008), and (11/2009) – Merck/JV Cholesterol Metabolism FBG-Superior Performance in Marketing and Leadership Principles, understanding the customer’s perspective and ensuring that execution is efficient, consistent, and well integrated

➢ Medical Education: o Designer, Cordis Cardiac and Vascular Institute, a source of educational and clinical resources including abstracts, articles, educational slide sets, clinical cases and eLearning programs for healthcare professionalso Prepared/reviewed several slide decks on disease states and therapeutic options – educated internal as well as cross-functional personnel.o Prepared specialized target decks to address topical issues/studies relevant to Cordis business products.o Reviewed multiple presentations for CEU implementation (nurses, technologists)o Reviewed proposal of program content for various education development projects.o Provided MAS training/support regarding disease states, therapies, and relevant publications.o Chair, CME Grant/Fellowship committee and assisted in development of committee SOPs.➢ Lead, Simulation training programs including Virtual Anatomy Training Program.➢ Lead, Data Dissemination for Carotid Launch Team, including slide set preparation, podium strategy, publication strategy, integration of Medical Information and Medical Communication messaging, sales training, and worldwide informational webcasts – received J&J Encore Award for Excellence in Performance.➢ Lead, Publication and Podium Strategies across Franchises.➢ Medical Operations:o Developed departmental SOP’s including Protocol Review Committee. o Led development of Medical Information Systemo Reviewed/developed 73 slide set presentations (disease states, conference notes, publications).o Reviewed/analyzed 128 publication reprints for medical and scientific accuracy and appropriate dissemination.o Reviewed/developed 64 medical letters addressing commonly asked questions by medical providers regarding a variety of disease states and applicable recent literature.➢ Extensive collaboration with Health Economics group, CMS ➢ Team Leader, Response to AHRQ - received J&J Encore Award for Excellence in Performance.

➢ Devised an on-line training program (revised Medical/Legal Reference Manual) outlining the roles and responsibilities of all M/L Board members with a focus on promotion manager’s presentations.➢ Devised training program for sales managers to ensure accurate presentation of Product Circular information to customers/clients. ➢ Course Organizer/Presenter – The Content and Format of a Clinical Study Report/Common Technical Document.➢ Medical Affairs – Member of Medical/Legal Review Board responsible for the review of materials (ZOCOR, ZETIA, VYTORIN) used in worldwide promotion to physicians, pharmacists, managed healthcare providers, other healthcare professionals, and consumers – detail pieces, obstacle handling materials, bulletins to the field, reprints, computer-based detailings, tele-detailing, e-detailing, TV ads, materials/booths for major scientific meetings, and internet sites. Interacted extensively with DDMAC and familiar with NCQA-HEDIS Performance Navigators. Ensured that Merck’s promotional activities are scientifically accurate and comply with regulatory standards while also meeting promotional needs.➢ Responsible for all editing activities associated with the critical scientific review and final approval of clinical documents for inclusion in worldwide marketing and product licensing applications.➢ Co-author and Reviewer of numerous Medical Affairs Policies and Procedures.➢ Member, Medical Affairs Policies and Procedures Committee on the Authoring and Review of Regulatory Documents➢ Chairperson/member of Worldwide Product Circular Review Committee (WPCRC) ➢ Member, Molecular Targeting/Imaging Task Force.➢ Member, Adverse Experience Review Team, Project Team, and Labeling Task Force for assigned products.➢ Reviewer, Merck literature proposed for publication/presentation for assigned products.➢ Member, Global Regulatory Teams, Global Regulatory Policy Network, Careers and Competencies Development Team.➢ Member, ZETIA launch team

➢ Member, Worldwide Business Strategy Team (CNS franchise) ➢ Member, Commercialization Sub team (CNS franchise).➢ Prepared Merck’s first-ever clinical trial bridging strategy document (CNS drug) for submission to the Japanese Regulatory Agency.➢ Prepared and presented the regulatory strategy for Merck’s entire Chemoprevention program to the EMEA ➢ Author, Standard Operating Procedure for the Export Petition Application process.➢ Responsible for the management of the worldwide regulatory development of anti-inflammatory compounds (OA, RA JCA, Alzheimer’s, Mild Cognitive Impairment, GI Endoscopy, Chemoprevention) ➢ Supported International filing of anti-inflammatory compound and lead international filing of associated Outcomes trials.➢ Responsible for the management of the regulatory development of several CNS compounds (Migraine and Alzheimer franchises) ➢ Successfully negotiated critical label contents for CNS drug with the Canadian Regulatory Agency ➢ Successfully negotiated with Switzerland Agency gaining exclusive first-line indication and dosage recommendation for MAXALT.➢ Global Regulatory Team Leader for MAXALT franchise.➢ Member, Global Regulatory Strategic Review Committee.➢ Successfully completed multiple Type I and II variation Procedures ➢ Merck Research Laboratories recruiting Representative at American College of Physicians Meeting, April 2000.➢ Principal organizer of Worldwide Regulatory Affairs Annual Meeting 2000 – received Merck Award for Excellence for Planning, organization, and management, 12May2000.➢ Member of Document Review Committee, COX-2 Outcomes Research Team, CSA/WMA Tracking Team.➢ Reviewed multiple protocols (pediatric/adult, international/domestic), Data Analysis Plans, Basic Medical Plans, and Clinical Study Reports.➢ Maintained current knowledge of the registration requirements in various countries including the United States and provided guidance to project teams as to these requirements.

➢ Educated Professional Representatives, National Account Executives, product specialists, and others about Bracco products and business specific medical diseases➢ Provided analyses of pertinent medical literature ➢ Developed product monographs, monographs regarding disease entities, comprehensive bibliographies, collections of articles, presentations, and multimedia programs for customers➢ Developed innovative medical educational programs and clinical trial initiatives with key opinion leaders, academic institutions, professional societies, and other medical groups➢ Lectured on medical topics and products to various internal and external groups➢ Presented at Sales training seminars (on and off-site) to further knowledge of Sales staff➢ Presenter at several major scientific and marketing meetings (U.S. and International)➢ Developed and disseminated special reports on key marketing and other product issues➢ Developed and managed strategic relationships with key opinion leaders➢ Directly managed the company’s top priority, multi-center, Cardiovascular clinical development project➢ Extensive oral presentation experience to diverse audiences (including Grand Rounds, resident/student education, administrative, continuing medical education to colleagues)➢ Principle Reviewer of correspondence with the FDA (CDER) with direct responsibility for medical responses to Agency questions➢ Chairman, Committee for Review of External Protocols and Study Proposals➢ Member, Discovery Team for New Products➢ Member, Evaluation Team for New Corporate/Product Acquisitions➢ Member, Medical/Legal Review Team➢ Development and preparation of protocols, case report forms, and worldwide labels➢ Medical/Clinical representative in development and implementation of NIK/NCI International Breast Cancer Detection Consortium Study➢ U.S. Medical Representative, International Task Force Team for Globalization of the Clinical Development Process➢ Consultant to Medical Safety Division.

➢ Supervisor of twenty technologists, six office staff; directly responsible for quality assurance, professional services, and statistical analysis of business trends.➢ General radiology and ultrasonography.➢ Responsible for strategic business and development plans.➢ Responsible for recruitment of personnel and staff continuing medical education.➢ Responsible for equipment maintenance and acquisition – quality assurance, quality control.➢ Instituted teleradiology system enhancing efficiency in delivery of patient care.➢ Contributor, Long Range Operating Plan

➢ Director, Radiology Education for Residents and Medical Students.➢ Best Interdisciplinary Teacher Award, Obstetrics/Gynecology Residency Program, 1992➢ Member, Institutional Review Board for the Transitional Year Internship Program.➢ Section Chief, Ultrasound Division - Responsible for Quality Assurance Monitoring, Staff Continuing Education, and Equipment Maintenance and Acquisition.➢ Contributor to business development strategy➢ Advisor, Temple medical students, residents