global medical affairs resume example with 5+ years of experience

(555) 432-1000,
Montgomery Street, San Francisco, CA 94105
Professional Summary
Highly motivated Sales Associate with extensive customer service and sales experience. Outgoing sales professional with track record of driving increased sales, improving buying experience and elevating company profile with target market.
  • Guest services
  • Inventory control procedures
  • Merchandising expertise
  • Loss prevention
  • Cash register operations
  • Product promotions
St. Vincent's Medical Center New York, NY Expected in Present License# PCT.0013475 : - GPA : Pfizer Postdoctoral Fellow, Global Medical Affairs PGY-1 Pharmacy Resident/ Licensed Pharmacist
University of Connecticut Storrs, CT Expected in May 2015 Doctor of Pharmacy : - GPA :
, Expected in May 2013 Bachelor of Science : Pharmacy Studies - GPA : Pharmacy Studies
University of Beijing Beijing, Expected in May 2012 B.A : Molecular and Cell Biology - GPA : Molecular and Cell Biology
Work History
Covenant Healthcare - Global Medical Affairs
Saginaw, MI, 06/2016 - Current
  • Rutgers Pharmaceutical Industry Fellow, Global Medical Affairs Fellowship in Global Medical Affairs with deliverables in medical strategy, clinical pharmacology, safety, commercial, medical/legal/regulatory approvals and business development across therapeutic areas HCP Engagement and Digital Strategy.
  • Project lead on digital strategy piloting the development and dissemination of KOL digital conference highlights at national and international congresses.
  • Responsible for agency selection and management, content creation, KOL contracts and engagement.
  • Delivered digital content to 11 countries, reaching over 60,000 HCPs within 24 hours of their presentation at the European Congress for Neuropsychopharmacology (ECNP).
  • Managed Medical/Legal/Regulatory approvals.
  • Partnered with colleagues across disciplines and countries to collect key performance indicators; presented best practices to senior leadership.
  • Formulated a collaborative agreement and acquired partnership with an international psychiatric organization (ECNP).
  • Interfaced with international thought leaders and professional organizations (APA & ECNP).
  • managed scientific collaborations, speaker training, advisory boards, and regional/national/international conferences Commercial.
  • Primary point of medical contact to global commercial team to provide appropriate medical input for promotional pieces, support in-market launch activities and strategic medical input for CNS assets HEOR Authorships:.
  • Health and economic burden of under treated depression among patients with cardiovascular disease (CVD) using a US retrospective claims database".
  • Performed data analysis, developed study design, selected cohorts and defined endpoints.
  • A real-world study on time-to-initiation and dose optimization of major depressive disorder treatment in the United States".
  • Assessed time to therapy initiation and time to reach minimum therapeutic dose (MTD) in patients receiving SSRI or SNRI for Major Depressive Disorder.
  • The Economic Impact of Hospital Antimicrobial Stewardship Programs".
  • Reviewed and analyzed the cost/benefit of ASPs in key markets (such as EU and US) Scientific Medical Communication.
  • Spearheaded strategic implementation of a highly utilized global digital library of CNS content across therapeutic areas adapted across regions and digital channels.
  • Created medical content and implementation guide based on local market characteristics with premade communication plans and email communications for local repurposing.
  • Managed agency partners to ensure the proper medical review of materials prior to submission to regulatory and legal approval Clinical Pharmacology.
  • Conducted a pivotal phase 1 randomized bioequivalence study to support registration of a PDE-5 Inhibitor in China in collaboration with global, cross functional teams: statistics, clinical pharmacology, research and development.
  • Supported NDA submission and met bi-weekly with study team to ensure high quality of data.
  • Key player in the development of the Statistical Analysis Plan (SAP), Safety Review Plan (SRP) and Clinical Study Report (CSR) Business Development.
  • Provided value proposition for a phase III, characterized oral desensitization immunotherapy agent (CODIT); cross functional engagement with EU payers, commercial, business development and medical.
  • Mapped unmet medical need, opportunity cost, competitive positioning (existing and future), generics, pricing, access, competitive landscape and pipeline considerations.
  • Performed in-depth review of clinical/regulatory/safety data and market research through Q&A with EU Senior Management.
  • Key discussion points included:.
  • Launch plan, including priority markets and information on key customer targets.
  • Market access plan and information on expected pricing, reimbursement landscape.
  • Perspectives on product profile relative to competitors such as ViaSkin Safety: Decision Analysis Tool for Executive Benefit Risk Committee.
  • Developed and launched a portfolio of educational materials on Multi-Criteria Decision Analysis (MCDA) for the CMO's corporate-wide initiative based on a survey of cross-functional colleagues concerning tofacitinib.
  • Piloted benefit risk conferencing, produced animated video as a case study featured on internal micro-website and created an in-depth report with reference documents Medical Strategy.
  • Developed medical and digital strategies for unbranded programs with regional and country leads.
  • Led workgroups with the Pfizer Pharmacist Association and Medical Strategy Committees to explore organic growth utilizing "Dare to Try" framework, a selective program aimed at supporting an innovative mindset among Pfizer employees.
  • Supported interactions with thought leaders and professional organizations including scientific collaborations, speaker training, advisory boards, and regional/national/international conferences Research Publications Health and economic burden of under treated depression among patients with cardiovascular disease (CVD) using a US retrospective claims database.
  • Pfizer Inc.
  • June 2017.
  • Roger McIntyre, MD, Elizabeth Pappadopulos, PhD, Ahmed Shelbaya, MD.
  • Jessica, Claire A real-world study on time-to-initiation and dose optimization of major depressive disorder treatment in the United States.
  • Pfizer Inc.
  • June 2017.
  • Elizabeth Pappadopulos, PhD, Rita Prieto, MD, Matthieu Boucher, PhD, Ahmed Shelbaya, MD.
  • Jessica, Claire Celecoxib for the treatment of ankylosing spondylitis.
  • Journal of Rheumatology and Arthritic Disease.
  • Pfizer Inc.
  • Jessica, Claire, Chris Walker, PhD, Jian Zhu MD.
  • January 2017.
  • MTM Considerations in Osteoporosis Care: Current Issues for Prevention and Treatment.
  • Drug Topics.
  • Vol.
  • 157, No.
  • 10.
  • October 2013.
  • Fei Wang, Claire, Jessica, Claire, Audrey Corman, Claire, Joshua Baldino, Claire.
St. Vincents Medical Center - PGY-1 Pharmacy Resident
City, STATE, 06/2015 - 05/2016
  • Properly filled and dispensed an average of [number] prescriptions per day.
  • Effectively resolved insurance rejections and other billing issues.
  • Managed approximately [amount] dollars in cash and credit card sales daily.
Additional Information
  • Honors and Awards Dare to Try Champion, Pfizer Inc. March 2017 P4 APPE Excellence in Communication Award May 2015 ASHP Clinical Skills Competition Semi-Finalist October 2014 Joseph L. Sewall Memorial Pharmacy Scholarship August 2014 Cardinal Health Full Pharmacy Scholarship May 2014 NCPA National Member of the Year March 2013 Bill Gates Millennium Scholarship Aug. 2007 - Aug. 2012 Rhode Island Foundation Scholarship Aug. 2007 - Aug. 2012 2 Jessica, Claire

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Resume Overview

School Attended

  • St. Vincent's Medical Center
  • University of Connecticut
  • University of Beijing

Job Titles Held:

  • Global Medical Affairs
  • PGY-1 Pharmacy Resident


  • License# PCT.0013475
  • Doctor of Pharmacy
  • Bachelor of Science
  • B.A

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