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Stellenbeschreibung Role Summary ·       The Medical Advisor holds primary responsibility within the country for the development and execution of the Medical Affairs strategic plans and is expected to spend up to 50% of their time in external engagements. • The role focuses on cross-functional strategy collaboration and execution, building trust with the medical/scientific community, facilitating peer-to-peer medical and scientific exchange, and providing asset issue resolution support. Responsibilities and Primary Activities Asset Management & Business Leadership ·     Consolidates actionable medical insights from the country that can help inform company strategies ·     Translates Global Medical Goals and Strategies into research, data analysis, scientific communication, education, and other solutions that improve patient outcomes and enhance access in their country ·     Follows up on investigator-initiated study proposals they receive that are aligned with the MISP (Investigator Studies Program) areas of interest as per guidance and instructions in the MISP manual ·     Supports execution of and quickly adapts tactical plan to business realities in country ·     Acts with ethics and integrity; provides non-promotional, balanced, reliable, and scientific information; follows strictly company standards and local regulations Scientific & Technical Leadership ·     Infuses country’s scientific and healthcare environment perspective into Regional Medical Affairs Team ·     Communicates both scientific and business needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels ·     Builds trust with external scientific community via peer-to-peer scientific exchange, research, and educational collaborations, and via interactions with scientific societies, health organizations, publications, etc. ·     Provides therapeutic/functional training to assigned teams and affiliate functions ·     Develops and executes country medical educational programs and symposia ·     Leads country advisory boards and expert input forums to inform company strategy ·     Participates in and contributes significantly to professional organizations and academic or regulatory working teams Asset Regulatory Management ·     Successfully collaborates with and leads resolution of Regulatory, Reputational (i.e., Public Relations), Compliance, and other asset issues management ·     Collaborates in the successful management of asset safety or quality issues (i.e., contributes content and strategy in regulatory responses and interactions, risk management planning, and implementation) Medical Information ·     Provides prompt medical information support, such as research and answering of medical inquiries from external and internal customers, and reviews/approves local response documents Required Qualifications, Skills, & Experience Minimum ·     MD (Medical Doctor), with PhD or Master Degree is an advantage ·     Recognized expertise through 2-3 years of clinical and/or research experience in therapy area ·     Experience with local pharmaceutical industry guidelines, regulatory/reimbursement framework, and clinical research guidelines ·     Ability to think strategically, specifically in relation to asset value proposition and clinical and value evidence ·     Ability to develop a network of scientific leaders and successful interactions with other key stakeholders (public groups, government officials, medical professional organizations) in therapy areas ·     Proven ability to effectively communicate information at country management level, with public groups and to scientific leaders ·     Excellent interpersonal, analytical, communication (written and oral), and results-oriented project management skills ·     Strong prioritization skills and ability to understand how decisions fit into the broader context of corporate strategies ·     In a matrix environment, ability to effectively collaborate across functions Required Skills: Anpassungsfähigkeit, Anpassungsfähigkeit, Asset-Management, Berufliche Integrität, Bildung im Gesundheitswesen, Datenanalyse, Klinische Forschung, Medical Affairs, Medizinische Kenntnisse, Medizinische Kommunikation, Medizinische Kontrolle, Medizinische Texte schreiben, Optimierung des Projektmanagements, Pharmazeutische medizinische Angelegenheiten, Prioritätensetzung, Produktrisikomanagement, Projektmanagement, Projektmanagement-Unterstützung, Prüfung von Marketingmaterialien, Public Relations (PR), Regulatory Management, Risiko-Management, Strategische Planung, Strategisches Denken, Technische Führung {+ 1 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Personalberatungsvertreter, bitte sorgfältig lesen Merck & Co., Inc., Rahway, NJ, USA, auch als Merck Sharp & Dohme LLC, Rahway, NJ, USA, bekannt, akzeptiert keine unaufgeforderte Unterstützung von Personalvermittlungsfirmen. Alle Lebensläufe, die von Personalberatungen an einen Mitarbeiter unseres Unternehmens gesendet werden, ohne dass eine gültige schriftliche Vermittlungsvereinbarung für diese Position besteht, gelten als alleiniges Eigentum des Unternehmens.  Im Falle der Einstellung eines Bewerbers durch unser Unternehmen in Folge einer Agenturempfehlung wird keine Gebühr entrichtet, sofern keine entsprechende vorherige Vereinbarung besteht. Wenn Vereinbarungen mit der Agentur vorhanden sind, sind die Einführungen positionsspezifisch. Bitte keine Anrufe oder E-Mails. Mitarbeiter-Status: Fest angestellt Umzug: Visa-Sponsoring: Reiseanforderungen: Flexible Arbeitszeitvereinbarungen: Hybrid Schicht: Gültige Fahrerlaubnis: Gefahrstoff(e): Job Posting End Date: 08/23/2026 *A job posting is effective until 11:59:59PM on the day BEFORE  the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.