Kim Premo Email and Phone Number

Field-based professional with scientific, clinical and Oncology expertise responsible for providing medical and scientific support for AstraZeneca's products, new indications for current products and compounds in development. Engages in scientific exchange with thought partners consistent with Medical Affairs and Therapeutic Brand Teams' objectives.• Identify and develop relationships with key External Scientific Experts (ESE) in Northern Manhattan, Upstate NY, Connecticut and Rhode Island.• Developed a territory planning and documentation spreadsheet tool for Global and US Oncology MSLs (rolled out 2016)• Developed and lead training on CiteLine® resources and SiteTrove® for Oncology team to assist team with key initiatives and territory planning (rolled out in 2015 and developed an enduring resource with CiteLine® for onboarding)• Training lead for Lung Sub-Team througho Developed lung cancer onboarding ramp up guide for new Lung MSL team in December 2014• MSL Lead for ECOG-Acrin engagement and strategic collaboration plan• Co-Lead for ASCO 2016 for Oncology MSLs and ESE Engagement Lead for ASCO 2016o Participate on and coordinate with Global ASCO Operations and Planning teamo Organize and manage schedule for ESE Engagement activities for all US Based External Experts attending ASCO including but not limited to engaging and securing key internal stakeholders for specific meeting requests with ESEs.• Co-Chair of Oncology MSL Advisory Team• Active member, Medical Affairs Women’s Leadership Initiative (MAWLI)

• Identified, developed and/or enhanced relationships with Urology and Lung Cancer thought leaders in Upstate NY and Connecticut• Proactively resolved issues with cross-functional team members within Astellas and our Oncology partners at Medivation, Aveo Oncology, and Seattle Genetics.• Provided clinical information through scientific exchange to health care professionals.• Evaluated and trained members of Astellas speaker’s bureau • Supported Astellas’ sponsored research and investigator- sponsored clinical research proposals• Team Lead for collaborations with ECOG-ACRIN • Prostate Cancer Training Lead

• Responsible for the development and execution of a cross-functional Medical Affairs training strategy in support of the organization's business strategy and objectives in Oncology • Contributed as a member of the Oncology leadership, Core Medical, and brand leadership teams representing field and customer perspectives • Accountable for developing and managing 1.5 million dollar budget allocated for field Scientific Affairs therapeutic training resources• Conceived and developed the Field Director Coaching for Excellence resource guide to enhance coaching and development of medical liaison OL engagement skills and professional development• Collaborated with Legal and Regulatory and Health Care Compliance to develop and facilitate a mandatory case-based compliance skills program for Scientific Affairs Staff• Developed and facilitate a quarterly Essentials in OL Engagement Skills Course• Developed and implemented a case-based Advanced OL Engagement Skills workshop for Medical Liaisons

• Develop and enhance professional relationships with Hematology-Oncology thought leaders• Provide clinical and economic value information through scientific exchange to payors, formulary decision makers, and clinicians; identify and train members of Amgen’s speaker’s bureau and ensure they are updated on new data; facilitate submission of investigator sponsored pre-clinical and clinical research proposals; and support Amgen sponsored research. • Developed and executed journal club activities for Northeast team• Mentor new medical liaison team members• National RML Team Study Lead • Medical Meeting Planning Lead• Develop and execute plan for onboarding new hires• Institute Product Lead Advisory Committee • Develop Medical Meeting Lead process guide • Establish major medical meeting scientific booth activity database and outcomes report

I was responsible for the local and VISN 2 formulary project to ensure the formulary was consistent with national formulary and managed changes and monitoring of the products within formulary. I developed a process for requesting, logging and responding to non-formulary requests electronically. In addition to formulary work, I worked in the Coumadin Clinic and assisted with other clinical functions and staff clinical development.