Free
Medical Advisor, Seoul
Korea South, 서울, 서울,
게시됨 November 17, 2023
설명
Job DescriptionStrategic and Tactical LeadershipConsolidates actionable medical insights to inform company strategiesTranslates Global Medical Goals and Strategies into tactics and solutions that promote optimal scientific exchange aimed at helping improve patient outcomes and enhancing accessPromotes execution of and quickly adapts tactical plans to local business realitiesFollows up on Investigator-Initiated Study (IIS) proposals aligned with Our Company ISS Program areas of interestpartners with our research laboratories/Global Clinical Trial Operations (GCTO) personnel to identify potential investigators for our clinical development programsIn partnership with colleagues, facilitates the delivery of data generation activities (phases I-IV), including the identification of suitable research projects, research centers, investigators, and innovative methods to generate dataProvides non-promotional, balanced, and reliable scientific information following company standards and local regulationsMedical and Scientific LeadershipBrings the local scientific and healthcare environment perspective to the Regional Medical Affairs teamconveys scientific and business needs appropriately and effectively across internal and external stakeholdersBuilds reliance with the external scientific community via peer-to-peer scientific exchange, research, and educational collaborations, as well as interactions with scientific societies, health organizations, publications, etc.Provides therapeutic/functional training to assigned teams and affiliate functionsDevelops and executes country medical educational programs and symposiaSteers country advisory boards and expert input forumsParticipates in and contributes to professional organizations and academic/regulatory working teamsRegulatory and Market Access SupportPartners and steers resolution of regulatory, public relations, compliance, and other asset issuesBoosts the resolution of asset safety or quality issues (i.e., contributes content and strategy in regulatory replies and interactions, risk management planning, and implementation)Provides access sponsor as needed (e.g., health technology assessment, pre-license patient access, reimbursement dossier)