Executive Medical Director - US Medical - Obesity and Related Conditions

About the role

Join Amgen’s mission of serving patients. As the Executive Medical Director, US Medical Lead - Obesity & Related Conditions, you will lead the development and execution of the US Medical Affairs strategy for Amgen’s Obesity & Related Conditions portfolio, focusing on Chronic Weight Management (CWM) and Obstructive Sleep Apnea (OSA) indications.

Responsibilities

• Provide strategic medical leadership across medical launch readiness, evidence generation, external medical engagement, scientific communications, field medical alignment, and lifecycle planning.
• Contribute to product and portfolio strategy for Obesity & Related Conditions by providing medical and scientific input into launch readiness, lifecycle planning, evidence generation, and indication expansion priorities.
• Develop and lead execution of US Medical Affairs strategy, including external medical engagement, scientific communication, evidence generation, medical education, medical insights, and congress strategy.
• Serve as a close strategic partner to the Field Medical organization, including the National Leader for Field Medical, to align on medical strategy, scientific priorities, field medical resources, medical education needs, external expert engagement planning, and medical insight generation, while ensuring Field Medical activities remain independent, non-promotional, and compliant.
• Collaborate cross-functionally with Commercial, Value & Access, Key Account Management, Legal/Compliance, Regulatory, and other relevant functions, while maintaining Medical Affairs independence and ensuring activities remain scientifically appropriate and compliant.
• Develop and lead the US medical communication strategy, including clinical narrative framework, scientific platform, core medical content, congress materials, publications, field medical resources, and scientific exchange priorities.
• Engage US external stakeholders, including thought leaders, clinical experts, professional societies, payers, integrated delivery networks, accountable care organizations, and other relevant healthcare decision-makers, through appropriate, compliant scientific exchange to strengthen understanding of unmet need, disease burden, clinical evidence, and medical value.
• Provide medical and scientific input, as appropriate, into evidence-generation, health economics and outcomes research, and payer-relevant scientific discussions to support accurate understanding of disease burden, unmet need, clinical evidence, and appropriate use.
• Partner with Global Medical Affairs and cross-functional partners to ensure US medical needs are represented in global strategy, evidence plans, publication plans, and lifecycle medical planning.
• Lead medical insight generation and translate external medical, scientific, payer, and clinical practice insights into actionable recommendations for internal decision-making.
• Support US medical launch readiness and lifecycle medical planning for CWM and OSA indications through integrated medical planning and cross-functional collaboration.
• Elevate Amgen’s reputation as a science-based, patient-focused, and reliable partner in obesity, metabolic disease, and related conditions.
• Shape and execute integrated medical plans aligned with product, portfolio, and enterprise priorities.
• Serve as a strategic partner to the Field Medical organization and the National Leader for Field Medical to ensure field medical activities are aligned with the overall US medical strategy.
• Partner with Field Medical leadership to define scientific priorities, external medical engagement objectives, insight-generation needs, congress support, advisory board priorities, and medical education opportunities.
• Work closely with customer-facing areas to ensure aligned, compliant, and medically appropriate engagement across key stakeholder groups.
• Lead US external stakeholder strategy and engagement with experts in obesity, metabolic disease, sleep medicine, cardiometabolic disease, primary care, and relevant professional societies.
• Serve as a senior medical voice in cross-functional forums supporting medical launch readiness, lifecycle planning, and access-related scientific discussions.
• Lead, mentor, and develop Medical Affairs team members, fostering accountability, collaboration, inclusion, and high performance.
• Knowledge of Good Clinical Practices, US regulations, industry codes, and compliance requirements relevant to Medical Affairs activities.
• Strong understanding of pharmaceutical product development, product lifecycle, and commercialization processes, including Clinical Development, Commercial, Regulatory, Value & Access, Safety, Legal/Compliance, and Medical Affairs.
• Experience developing medical communication strategy, scientific platforms, clinical narrative frameworks, congress plans, publication plans, and core medical content.
• Experience translating medical insights and external stakeholder perspectives into actionable strategic recommendations.
• History of solving complex problems while exercising strong judgment, scientific integrity, and a balanced understanding of business, clinical, regulatory, and patient considerations.
• Demonstrated commitment to patient-centered decision-making, scientific excellence, and ethical leadership.
• Experience collaborating with integrated delivery networks, accountable care organizations, payers, health systems, professional societies, and other healthcare decision-makers.
• Experience developing or supporting digital channels and omnichannel scientific education strategies to enhance compliant medical education and scientific engagement.

Qualifications

• Doctorate degree & 6 years of medical affairs experience OR Master’s degree & 10 years of medical affairs experience OR Bachelor’s degree & 12 years of medical affairs experience AND 6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
• M.D., DO, Ph.D., or PharmD. from an accredited medical school, board certification or board eligibility in Endocrinology, Obesity Medicine, Internal Medicine, Pulmonology, Sleep Medicine, Cardiology, or another relevant specialty preferred.
• 8 or more years of experience in the biopharmaceutical industry, including Medical Affairs, Clinical Development, Clinical Research, or related functions.
• 5 or more years of Medical Affairs experience in the biopharmaceutical industry, ideally including US medical strategy, launch planning, evidence generation, and external stakeholder engagement.
• Deep understanding of obesity, chronic weight management, obstructive sleep apnea, cardiometabolic disease, and related complications or comorbidities.