AD​/Sr AD, Sci Affairs Med Info & Med Review; CRM, Obesity, MASH

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.

Associate Director (AD):
Responsible for the development, maintenance, and continuous improvement of U.S. Medical Information (MI) assets and serves as a Medical Reviewer on the Human Pharma Review Committee (HPRC), supporting MLR review of U.S. medical and promotional communications. Partners with Medical Affairs Strategy and Global MI to deliver accurate, scientifically balanced, and globally aligned content that meets customer and regulatory requirements. Ensures reviewed materials are scientifically sound, compliant, and consistent with FDA regulations and current medical standards while supporting processes, knowledge management, compliance, and cross-functional initiatives.

Primary support includes the Cardio-Renal-Metabolism (CRM) portfolio, including obesity, liver disease, and chronic kidney disease (CKD), with additional therapeutic areas assigned as needed.

Senior Associate Director (SAD):
In addition to AD responsibilities, the SAD provides leadership and advanced MI and Medical Review(MR) expertise. The SAD proactively contributes to and ensures alignment with medical and brand strategies, and drives continuous process and system improvement based on evolving customer needs.

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.

Associate Director (AD):
Responsible for the development, maintenance, and continuous improvement of U.S. Medical Information (MI) assets and serves as a Medical Reviewer on the Human Pharma Review Committee (HPRC), supporting MLR review of U.S. medical and promotional communications. Partners with Medical Affairs Strategy and Global MI to deliver accurate, scientifically balanced, and globally aligned content that meets customer and regulatory requirements. Ensures reviewed materials are scientifically sound, compliant, and consistent with FDA regulations and current medical standards while supporting processes, knowledge management, compliance, and cross-functional initiatives.

Primary support includes the Cardio-Renal-Metabolism (CRM) portfolio, including obesity, liver disease, and chronic kidney disease (CKD), with additional therapeutic areas assigned as needed.

Senior Associate Director (SAD):
In addition to AD responsibilities, the SAD provides leadership and advanced MI and Medical Review(MR) expertise. The SAD proactively contributes to and ensures alignment with medical and brand strategies, and drives continuous process and system improvement based on evolving customer needs.

Planning:

• Plans and prioritizes MI response content using customer inquiries, emerging evidence, and external trends, and provides actionable insights to inform cross-functional medical and business strategies.
• Applies medical review expertise early in content planning to advise project owners on material feasibility and provide solution-oriented guidance that supports submission of scientifically accurate, appropriately contextualized, and approvable content to HPRC.

Response Content Management:

• Develops and reviews Medical Information response content for external customers, including FAQs, Standard Scientific Response Content (SSRCs), customized responses, dossiers, and related training resources.
• Collaborates…