US Executive Director, Early Assets
Wilmington, DE - USA
Job Summary
Are you ready to turn ideas into life-changing medicines At AstraZeneca we are committed to addressing the unmet needs of patients worldwide through scientific this role you will play a crucial role in leveraging our scientific capabilities to positively impact patients lives. This is an opportunity to seize design and influence across a complex matrix system to ensure US needs are integrated into global development plans.
Accountabilities:
This role is accountable for the overall success of each Early Asset at the US level. It integrates clinical access and analytics strategies owns the US position in MC3 and other tollgates ensures market readiness optimizes enrolment of US patients in clinical trials and drives coherent decisions and deliverables that maximize the value and patient access of the Early Assets portfolio.
What Youll Do:
- Asset Strategy and Shaping: Define and pressure-test US-relevant target product profiles patient segments positioning hypotheses and differentiation strategies; ensure US needs are reflected in global asset plans and decision gates.
- Market and Customer Insights: Lead integrated US insight generation (secondary research qualitative/quantitative market research advisory boards rapid experiments) to inform clinical endpoints device/format choices and patient/physician usability needs.
- Access and Pricing Strategy: Shape early US payer value propositions evidence requirements and economic models; co-develop the early access and pricing roadmap with Market Access and HEOR to derisk future reimbursement.
- Cross-Functional Leadership: drive aligned recommendations into governance (e.g. TPP approvals go/no-go indication prioritization lifecycle planning).
- Competitive Strategy: Establish and maintain a dynamic competitive landscape assessment; identify opportunities for acceleration differentiation indication sequencing and combination strategies.
- Forecasting and Scenario Planning: Build and refine early forecasts and scenarios (epidemiology market adoption curves competitive events policy shifts); guide sensitivity analyses for stage-gate decision making.
- Go-to-Market Foundations: Define early brand identity and messaging hypotheses core claims framework and scientific narrative; prepare foundational resources to enable rapid and flawless transition to late-stage/launch teams input into initial field sizing assessment.
- BD and Alliance Support: Provide commercial diligence and market models for in-licensing partnerships and acquisitions; support alliance governance and joint working teams for partnered assets.
- Compliance and Ethics: Ensure all activities align with US regulations and company policies including pre-approval communication standards and interactions with external stakeholders.
- Policy: assess policy landscape and implications for design and launch
Minimum Qualifications
- Sophisticated Scientific Degree (MBBS PharmD PhD or MD) or international equivalent
- A minimum of 10 years in pharmaceutical healthcare or biotech industries
- A minimum of 3 years in early commercial new product planning or pipeline marketing; US market experience required.
- Strong scientific and business acumen
- Demonstrated experience in the innovative pharmaceutical industry with a strong track record in Market Access
- Ability to understand assimilate and communicate scientific information and Health Economic Outcomes data
- Demonstrated success shaping early-stage assets (Phase 12) and influencing clinical design and evidence strategy to meet future US access and adoption needs.
- Proven ability to lead without authority across Clinical Medical HEOR Market Access and Finance.
- Clear compelling communicator able to craft narratives for governance KOLs and internal stakeholders.
- Comfortable engaging with clinical data endpoints and mechanisms of action.
- Demonstrated ability to build trust and alignment across global and US stakeholders.
Preferred Qualifications
- Therapeutic area expertise in respiratory/immunology and CVRM strongly preferred (obesity/weight management experience highly preferred)
- Proficiency with market research design forecasting epidemiology inputs and competitive intelligence frameworks.
- Ability to identify innovative strategies with the greatest business impact and empower their teams to implement the plan.
- Strong curiosity growth mindset and high learning agility
- Comfort with NPV risk-adjusted forecasting scenarios and sensitivity testing for investment cases.
- Availability for occasional travel.
This position is based at our Wilmington DE campus headquarters for our US Biopharma we put unexpected teams in the same room we unleash bold thinking with the power to inspire life-changing -person working gives us the platform we need to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Next Steps Apply Today!
Are you ready to make a difference Apply now and join our mission to transform lives with our science!
The annual base pay for this position ranges from $331874 to $497810 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 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 offered included 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 the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired employee will be in an at-will position and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time including for reasons related to individual performance Company or individual department/team performance and market factors.
Date Posted
12-Jun-2026Closing Date
30-Jul-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and 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.
Required Experience:
Director
About Company
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more