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Medical Affairs Lead Stroke,HP ROPU ASKAN

THE POSITION

Throughout the lifecycle of Boehringer Ingelheim products, Medical Affairs lead will contribute to developing ROPU ASKAN Medico-Marketing strategies and collaborates in the implementation of the corresponding(R)OPU activities to achieve the Global Brand Plan (GBP)/Integrated Customer Plan(ICP)objectives. These strategies are part of a cross-functional effort (Medico-Marketing-Market Access interaction) to provide scientific guidance and clinically meaningful information, ensuring that the right patients can take advantage of the full benefits of Boehringer Ingelheim products. The strategies should help to drive the business for the Stroke portfolio at Boehringer Ingelheim.

 

Tasks & responsibilities

  • Lead the medical strategy for established products, ensuring continued clinical relevance and differentiation across the product lifecycle (Lifecycle Management (LCM) focus rather than new product launches).
  • Develop and execute medical plans supporting line extensions and new presentations, maximizing product value and patient impact.
  • Identify evidence gaps (clinical and real-world) and drive evidence generation plans in collaboration with RWE and Market Access to support access and value strategies.
  • Establish and maintain strategic partnerships with external experts (KOLs), ensuring high-quality, compliant scientific exchange.
  • Design and deliver medical education initiatives (e.g., symposia, workshops, train-the-trainer programs), ensuring scientific excellence and relevance.
  • Act as a scientific partner within cross-functional teams, contributing to integrated brand strategy alongside Marketing, Market Access, Regulatory, and other functions.
  • Provide actionable medical insights from external stakeholders to inform internal strategic decision-making.
  • Ensure alignment between local execution and regional (ASEAN/ASKAN) medical priorities.

 

Requirements

  • Doctoral degree (e.g. PhD, MD) in Medicine, Pharmacy or relevant area
  • Minimum of 3-5 years of solid experience in Medical Affairs, with proven project management capabilities, including work on established brands
  • Experience in neurology or emergency medicine is an advantage
  • Proven experience in cross-functional collaboration across regulatory and scientific activities and product lifecycle management
  • Scientific expertise with strong ability to apply medical knowledge and generate data-driven insights, particularly in pharmaceutical products
  • Strong business acumen combined with digital and data literacy
  • Effective stakeholder engagement, with strong communication, presentation, and negotiation skills
  • Demonstrated leadership, collaboration, and experience in evidence planning and generation, with high integrity and ethical standards
  • Strong analytical skills with a high level of attention to detailFluency in English is essential; proficiency in additional languages (e.g., Thai, Korean, or others) is valued and considered an asset

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