US Medical Head, Early Assets

AstraZeneca GmbH; Wilmington (DE); Presencial; USD 331.874 - 497.810; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

401(k) plan

Paid vacation and holidays

Health benefits

Descripción de la vacante

AstraZeneca is seeking a US Medical Head for Early Assets responsible for leading medical strategies for early pipeline therapies. This role emphasizes scientific leadership and collaboration across teams to shape the development of novel therapies.

Candidates should have a sophisticated scientific degree and over 5 years of experience in the pharmaceutical sector, particularly in CV and metabolism. The position offers competitive pay and an inclusive work environment.

Formación

• 5+ years of experience in the pharmaceutical industry or relevant health system setting.
• Proven track record to build internal/external networks.
• Substantial evidence generation/data expertise.

Responsabilidades

• Lead the US medical strategy for early pipeline assets.
• Act as the internal medical authority for emerging therapies.
• Drive the development of compelling scientific narratives.

Conocimientos

Deep medical expertise in CV and metabolism

Collaboration skills

Business leadership

Regulatory strategy knowledge

Educación

Sophisticated Scientific Degree (MBBS, PharmD, PhD, or MD)

Descripción del empleo

Introduction to Role

Are you ready to turn ideas into life-changing medicines? At AstraZeneca, scientific innovation drives everything we do to address unmet patient needs. In this role, reporting to the US Executive Director Early Assets, the US Medical Head, Early Assets leads ambitious US medical strategies for our early pipeline, shaping how novel therapies are developed and introduced. The role provides scientific leadership to cross‑functional teams, builds a strong external network across US disease areas where AstraZeneca has pipeline programs, and ensures US perspectives are embedded into global development plans. This is a chance to influence early asset strategy across a complex matrix, connect science with real‑world practice, and help set the course for future standards of care!

Accountabilities

• Lead the US medical strategy for early pipeline assets, ensuring alignment with portfolio priorities and long‑term business objectives.
• Act as the internal medical authority for emerging therapies, partnering closely with global medical, R&D, clinical, commercial, and market access colleagues.
• Develop robust translational and early clinical development plans that integrate medical insights, real‑world data opportunities, and evolving standards of care.
• Drive the development of clear, compelling scientific narratives that support outstanding launches and practice‑changing evidence.
• Guide study design elements such as endpoints, comparators, inclusion and exclusion criteria, and real‑world evidence strategies to enable future US access, labeling, and promotion.
• Build and maintain a comprehensive external engagement plan across key programs and disease areas, including leadership of medical advisory boards and strategic collaborations with external experts.
• Champion evidence generation activities across phases and data types to inform clinical decision‑making and support healthcare system adoption.
• Influence cross‑functional decision‑making by connecting insights from the healthcare ecosystem with internal strategy – asking bold questions, challenging assumptions, and turning ideas into action.

Essential Skills / Experience

• Sophisticated Scientific Degree (MBBS, PharmD, PhD, or MD) or international equivalent.
• 5+ years of experience in the pharmaceutical industry (medical, marketing, R&D, market access roles), or working in a relevant health system setting (clinical, pharmacy, pathway design etc.).
• Deep medical, clinical or scientific expertise in CV and metabolism (especially in obesity/weight management). Experience/knowledge in immunology and/or cell therapy also preferred.
• Experienced business leader able to deliver results in a complex matrix environment.
• US regulatory strategy knowledge including product approval, label requirements/negotiation.
• Proven track record to build internal/external networks and to collaborate internally/externally.
• Substantial evidence generation/data expertise, e.g. clinical trial experience (conducted P2, P3 or P4 studies), and/or substantial RWE experience.

Desirable Skills / Experience

• Global and/or R&D experience, or consistent track record of supporting early asset or first‑in‑class product development.
• Proven experience beyond medical affairs (e.g. in a marketing/R&D/market access role).

Working Environment and Office Requirements

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life‑changing medicines. In‑person working gives us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office, but remain flexible by respecting individual flexibility and balancing the expectation of being in the office.

Benefits and Compensation

The annual base pay for this position ranges from $331,874 to $497,810. Hourly and salaried non‑exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job‑related knowledge, skills, and experience. In addition, our positions offer a short‑term incentive bonus opportunity; eligibility to participate in our equity‑based long‑term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits include a qualified retirement program (401(k) plan); paid vacation and holidays; paid leaves; and health benefits including medical, prescription drug, dental, and vision coverage in accordance with terms and conditions of the applicable plans.

Equal Employment Opportunity

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.