Global Medical Indication Director

2 weeks ago


San Francisco, California, United States Argenx Full time
About Argenx

At Argenx, we're transforming immunology and delivering medicines that help autoimmune patients regain their lives. Our diverse pipeline of innovative assets is poised to reach more patients worldwide.

A New Era in Biotech

We're building a new kind of biotech company that balances its roots as a science-driven startup with a commitment to innovation across all aspects of our business. This vision inspires us to grow our company, partnerships, science, and people, ultimately delivering more for our patients.

The Role

This hybrid position will lead the clinical team for an indication, translating the Therapeutic Protein Profile (TPP) set by the Asset Strategy Team into a Clinical Development Plan that addresses relevant questions. The goal is to maximize the asset's potential for a given indication while ensuring time, quality, and budget are safeguarded.

Responsibilities
  1. Strategic Planning: Provide continuous strategic medical insight and planning for the indication throughout all development stages, owning the Clinical Development Plan and participating in long-range strategic planning as data emerge in the indication.
  2. Leadership: Line manage Global Clinical Trial Physicians working on the indication, coaching and setting examples to ensure high-quality medical support for study teams, identifying high performers for potential other roles.
  3. Study Oversight: Real-time oversight of the medical aspects of studies in the indication, including relevant communication to management and different study teams.
  4. Harmonization: Safeguard harmonization across studies to maintain consistent communications with external stakeholders and ensure company efficiency in close collaboration with peers and functional groups.
  5. Ad Boards: Lead indication medical ad boards as appropriate.
  6. Talent Development: Help build and maintain a 'best-in-class' group of development medical doctors.
  7. Compliance: Ensure compliance of all studies in the indication.
Requirements
  • Medical Background: Medical Doctor with relevant specialty education, immunology, or rheumatology, having acquired an in-depth understanding of end-to-end drug development based on relevant experience of at least 3-5 years in the pharma/biotech industry and clinical practice.
  • Language Skills: Excellent English skills, both written and spoken, with the ability to travel.
  • Leadership Skills: Proven leadership, motivational, and interpersonal skills in a global and intercultural environment, including leading through influence without direct reporting lines.
  • Problem-Solving: Proactive problem solver with negotiation skills.
  • Communication: Clear vision, direction, and purpose to different study teams, demonstrated expertise in clinical trial design, conduct, and interpretation of clinical data, strong communication skills to ensure transparency of study plans and status, risks, issues, and results.
Compensation

We offer a competitive salary range of $180,000 - $220,000, commensurate with experience, along with a comprehensive benefits package, including health insurance, retirement savings plan, and paid time off.



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