As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
The Senior Global Medical Advisor (SR GMA) designs the global Medical affairs strategy for the compounds and leads global strategic initiatives, providing guidance to regional and local medical initiatives. The incumbent is the medical ambassador for the asset to internal and external stakeholders. The position holder takes an active role in shaping the Evidence Strategy and Generation by working closely with the Evidence Lead and the Evidence Sub-Team.
In some cases, the SR GMA may assume the responsibility of an Evidence Lead in the Asset Teams, leading the creation and execution of a holistic evidence generation strategy and integrating the deliverables of all medical functions as the leader of the Evidence team. The incumbent will drive patient value, patient voice and quality of life & outcomes in line with Medicine Excellence goals.
Duties & Responsibilities Plans for medically adequate commercialization from early development throughout the whole asset life cycle.Contributes to the design of brand strategic goals to allow for efficient, scientifically and medically adequate commercialization efforts starting at early development until the end of the product's life cycle.The Medical Affairs strategy related to early pipeline compounds/indication/portfolio aims to contribute to the clinical development plans and overall evidence generation to ensure successful commercialization after launch and until the end of lifecycle.
Medical Affairs Planning & Execution:
External Expert Engagement & Scientific Leadership:
Accountable for expert identification & engagement, planning and executing advisory boards & consultancy meetings in cooperation with Scientific Relations, driving patient engagement in cooperation with Patient Advocacy Relations (PAR) and their respective plans.Represents BI and leads or takes active role at international scientific Advisory Boards, expert panels, round tables at Scientific Societies.
Competitive landscape analysis & scenario planning:
Requirements for Senior Global Medical Advisor
Advanced degree in Medical or Life Science, PhD.Accomplished industry professional with a broad knowledge of all phases of drug developmentMarket-relevant experience, including external stakeholder engagement in the therapeutic area (Global, Regional or local).Entrepreneurial mind-set and passion to build the asset for success.For early Medical Affairs: Past exposure to all the activities involved in successfully developing and launching assets and brands.Sound therapeutic area background with a minimum of ten (10) years in the Pharmaceutical Industry (Medical Affairs and/or Clinical Development roles, roles in combination with market knowledge and savviness, Management experience considered a plus).For roles in Early Medical Affairs: Track record in product launch activities in the medical function.Medical and scientific leadership to drive high-priority projects in collaboration with global matrix teams, regional/local counterparts and external partners.Requirements for Global Medical Advisor
MD, PhD or similar (specialist in the respective Therapeutic Area) from an accredited institution.With preferably two to five (2-5) years of experience in the Pharmaceutical Industry (Medical Department).Successful track record in planning, conducting and publication of Basic Science and/or Clinical Research.Sound medical and scientific leadership to drive high-priority projects in collaboration with global matrix teams, regional/local counterparts and external partners.
Eligibility Requirements:
Additional Duties & Responsibilities:
Patient benefit & Payor value:
Closely cooperates with the Market Access/HEOR colleagues to establish the pharmacoeconomic value of the compound, contribute to payer engagement and integrated healthcare solutions as well as developing programs to grant patients with no further therapeutic options early access.
Evidence & insights Generation:
Cross-functional cooperation: