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Global Medical Unit N&I Medical Director - Lupus

Merck Group
United Statesfull_timeVerifiedPosted 4 Sept 2025
💰 $252,100/yr($168,100/yr$252,100/yr)

About the role

 

Work Your Magic with us! Start your next chapter and join EMD Serono.

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 

Your Role: 

We are seeking a collaborative and motivated individual to join the Global Medical Unit (GMU) Neurology & Immunology (N&I) team as a Medical Director focused on lupus. This role is pivotal in building, monitoring, tracking, managing, and assisting with the implementation of GMU strategic initiatives. The Medical Director (all genders) will provide scientific and medical leadership from pre-launch through the entire product life cycle, particularly in support of the development of enpatoran program and a robust lupus franchise.

Key Responsibilities

Integrated Evidence Strategy:

  • Execute the Integrated Evidence Plan (IEP) aligned with the scientific narrative, positioning, and Target Product Value Proposition (TPVP).
  • Consider a broad scope of data sources, including clinical trials, phase IV programs, registries, and real-world evidence (RWE).
  • Develop 'Go/No-Go' criteria to guide country organizations in discussions with local investigators regarding Investigator-Sponsored Studies (ISS).
  • Integrate external and internal insights to create scientific questions that align with behavioral change concepts in physicians, patients, and allied healthcare professionals (HCPs).
  • Identify deficiencies, needs, or improvements in data/knowledge required to achieve product goals in lupus therapy areas.
  • Conduct critical reviews and provide input on data used in content creation.
  • Identify key points along the patient journey where data could influence clinical decisions and ensure data gaps inform innovative evidence generation and subsequent clinical trial design.
  • Approve sources of evidence for non-clinical and clinical studies funded by GMU team, in accord

HCP Insight Specialist:

  • Collect insights and create and implement action plans to reveal key insights that support clinical decision-making.
  • Transform raw data into compelling stories that drive change and work cross-functionally to embed insights into key initiatives.
  • Monitor external trends and events to anticipate opportunities and threats relevant to medical affairs.
  • Plan, run, and synthesize insights from advisory board meetings to gather feedback from external experts regarding the asset's development, positioning, and use in clinical practice.

Scientific Narrative Strategist:

  • Develop the scientific narrative in alignment with the TPVP, IEP, and asset strategy.
  • Coordinate internal alignment and integrate feedback for the scientific narrative.
  • Seek external validation of the scientific narrative and implement feedback.
  • Ensure the scientific narrative remains current with the latest information and is segmented to cater to different internal and external stakeholders.

Field Medical Material & Training Specialist

  • Design and produce high-quality, scientifically accurate materials, such as slide decks, brochures, and FAQs, tailored to the needs of field-based medical teams.
  • Ensure all materials comply with regulatory standards, legal requirements, and industry codes of practice, including accurate representation of clinical data.
  • Collaborate with medical, clinical, and commercial teams to align field materials with product strategies and clinical evidence.
  • Manage the review and approval process for medical field materials, ensuring timely distribution and availability.
  • Monitor and incorporate feedback from f

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Company

Merck Group

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