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US Medical Director – Immunology

Job in Germany, Pike County, Ohio, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-03
Job specializations:
  • Science
    Medical Science Liaison, Medical Science
Salary/Wage Range or Industry Benchmark: 180000 - 200000 USD Yearly USD 180000.00 200000.00 YEAR
Job Description & How to Apply Below
Location: Germany

US Medical Director – Immunology

$193K

At Astra Zeneca , we are committed to turning scientific innovation into life-changing medicines for patients. The US Medical Director – Immunology plays a pivotal role in shaping and advancing the US medical strategy for IV/SC and its lifecycle management indications, including systemic sclerosis (SSc),
cutaneous lupus erythematosus (CLE),
lupus nephritis (LN), and
idiopathic inflammatory myopathies (IIM).

Reporting to the US Medical Head, Immunology , this role is a core member of the US Medical Team Immunology and will help define the scientific narrative, evidence generation plans, launch readiness activities, and scientific communications strategy in the US. This is a highly visible, cross-functional leadership opportunity that will directly influence how scientific data is translated into meaningful medical impact for clinicians, patients, and the broader healthcare community.

Key Responsibilities
  • Co-shape and execute US medical strategy for lifecycle management , ensuring alignment with broader business and medical priorities.
  • Develop and communicate the US scientific narrative across indications, translating complex clinical and scientific data into clear, accurate, and compliant strategies and materials.
  • Support launch readiness for lifecycle indications, including scientific platform development, congress planning, internal training, scientific response planning, and medical information preparedness.
  • Partner on evidence generation strategy , including
    real-world evidence (RWE),
    health economics and outcomes research (HEOR),
    externally sponsored research (ESRs), publication planning, and congress activities.
  • Contribute to external scientific engagement plans with key experts, institutions, professional societies, and other stakeholders in a compliant and strategic manner.
  • Provide medical review and scientific input for publications, training materials, FAQs, and promotional and non-promotional content in collaboration with cross-functional teams.
  • Deliver scientific and clinical training for Field Medical teams and internal stakeholders to build readiness across lifecycle priorities.
  • Collaborate closely with global teams to ensure US insights and needs are reflected in global medical and development plans.
  • Ensure full compliance with FDA ,
    OPDP ,
    PhRMA , and Astra Zeneca policies, standards, and ways of working.
  • Champion innovative and AI-enabled ways of working to improve efficiency and enhance medical impact.
Must-Have Qualifications
  • An advanced degree such as MS, MD, PhD, or PharmD
    .
  • A minimum of 5 years of experience in medical affairs ,
    clinical development , and/or lifecycle management within the pharmaceutical, biotechnology, or academic sectors.
  • Strong expertise in immunology ,
    rheumatology ,
    autoimmune disease , or a closely related therapeutic area.
  • Solid understanding of the US regulatory and compliance environment , including FDA and OPDP requirements.
  • Experience contributing to evidence generation ,
    RWE/HEOR ,
    publications ,
    congress strategy , and scientific communications
    .
  • Demonstrated ability to work effectively in a cross-functional matrix environment and align US and global medical priorities
    .
  • Excellent scientific communication ,
    presentation , and stakeholder engagement skills.
  • The ability to translate complex scientific information into clear, compelling, accessible, and compliant messages for diverse audiences.
  • Strong judgment ,
    collaborative leadership , and a commitment to high ethical standards
    .
  • Willingness and ability to travel within the US and occasionally internationally
    .
Desirable Qualifications
  • Prior experience supporting launch readiness for new indications or lifecycle expansion opportunities.
  • Experience working across multiple stakeholder groups, including Medical ,
    Commercial ,
    Clinical Development ,
    Regulatory ,
    Market Access/HEOR ,
    Medical Information , and Patient Safety
    .
  • Familiarity with building or refining scientific platforms and medical response strategies
    .
  • Experience engaging with external experts ,
    institutions , and professional societies in a compliant scientific exchange setting.
  • Interest in or experience with innovative and…
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