Sr. AD, Medical Affairs Strategy Team Member

Description

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, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

The Senior Associate Director, Oncology Medical Affairs Strategy Team Member,  serves as the subject matter expert for assigned product to create the indication-specific or product-specific medical strategic framework and prioritized medical tactics to ensure the success of the respective BI product(s) from a Medical Affairs perspective, both prior to and leading up to launch, as well as throughout the product lifecycle.

This individual will bring together strong scientific knowledge of the therapeutic area, strong command of the relevant clinical practice guidelines and related scientific data, as well as the understanding of the overall TA priorities and value drivers into an integrated strategic medical plan and tactics that enable the successful medical affairs contribution to BI’s portfolio and informs clinical development efforts where applicable.

The Senior Associate Director, Medical Affairs Strategy Team Member, collaborates cross functionally within the larger Clinical Development & Medical Affairs (CDMA) department (e.g., Medicine Excellence, Field Medical Affairs, RWE, Publications, etc.) and across the organization (e.g.,Marketing, Market Access, Analytics & Insights (A&I), HEOR, Clinical Operations, Patient Services, Legal, Compliance, etc.) and with global counterparts to create, execute, measure and adapt the Medical Affairs strategy to best fit the needs of the US clinical landscape and market dynamics of relevance to the respective TA.

Duties & Responsibilities

• Partners with US and Global teams to develop launch strategies and integrated evidence plans that address key evidence gaps for assigned oncology products.
• Executes medical tactics, data releases, and evidence-generation initiatives aligned with BI/CDMA objectives, clinical development, and the evolving US healthcare landscape.
• Collaborates across Medical, Commercial, GTM, CDMA, and Clinical Development teams to support asset planning, launch readiness, and lifecycle strategy.
• Drives medical strategy by identifying opportunities and risks, incorporating stakeholder insights, and aligning cross-functional execution.
• Leads publication, scientific communication, congress, and medical education strategies to maximize the impact of clinical and scientific data.
• Designs and leads advisory boards, expert engagements, and insight-generation activities that inform strategic decision-making.
• Applies omnichannel engagement approaches to optimize scientific exchange, medical education, and evidence dissemination.
• Partners with internal stakeholders to optimize budget planning and advance digital, hybrid, and omnichannel capabilities.
• Represents the CDMA TA team in business planning and governance activities, helping define strategic priorities, KPIs, and success measures.
• Leads TA-specific strategic initiatives that enhance business agility, customer focus, and compliance.
• Develops medical tools, materials, and communication strategies for organized customers, Payers/Systems, and AMAs in collaboration with Value/Access and Health Systems teams.

Requirements

• Bachelor’s degree required, and in addition fulfill one of the following education levels:
• Seven (7) years of professional experience in a scientific, clinical, and/or medical affairs space, including five (5) years in relevant strategic position in pharmaceutical or related industry.
• One-plus (1+) years of experience in Medical Affairs, Clinical Trials, Regulatory, or related area supporting oncology therapeutic area
• Experience in neuroendocrine neoplasms, including small cell lung cancer (SCLC), extrapulmonary neuroendocrine carcinomas (epNEC), rare tumors, and related disease areas strongly preferred
• Demonstrated experience with pharmaceutical drug development and the use of data analysis for strategy development, business process improvement, product launch planning, and integrated evidence generation required.
• Demonstrated success leading publication and scientific communications programs, inclu