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Scholar Rock
4h ago

Country Medical Director(m/w/x)

Frankfurt am Main, München
Full-timeOn-siteSenior

Description

You will drive the medical strategy in Germany, leading a dedicated team to advance scientific leadership in rare diseases while fostering vital relationships with key stakeholders.

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Requirements

  • •MD, PharmD, PhD or equivalent scientific degree
  • •Minimum 7 years industry R&D experience
  • •Line Management experience
  • •Excellent communication and organizational skills
  • •Medical Affairs track record in biotech/pharma
  • •Native or Business Fluent German
  • •Fluent in English
  • •Scientific communication and presentation skills
  • •Leadership skills and adaptability
  • •Collaborative and proactive attitude
  • •Integrity and commitment to ethics
  • •Experience in rare diseases or SMA
  • •Success in product launches
  • •Clinical trial design experience
  • •Ability to evaluate business opportunities
  • •Successful partnership with Commercial organizations
  • •Curious learner focused on patient outcomes
  • •Team player with cross-departmental expertise
  • •Critical thinker with fact-based opinions
  • •Ability to simplify complex science
  • •Solid business acumen
  • •Results-oriented with can-do culture
  • •Scope for personal growth
  • •Mentorship and line report development

Education

Master's degree
OR
Doctoral / PhD

Work Experience

7 years

Tasks

  • •Provide strategic medical leadership for launch plans
  • •Identify unmet medical needs and data gaps
  • •Lead the country medical team and advisors
  • •Educate and gain insights from external stakeholders
  • •Engage with government agencies and medical societies
  • •Organize expert advisory boards and CME programs
  • •Report field medical insights through CRM systems
  • •Inform cross-functional strategies with medical insights
  • •Manage external vendors for medical content development
  • •Provide editorial support for data dissemination
  • •Review promotional and scientific materials
  • •Act as subject matter expert for internal groups
  • •Optimize clinical study protocols for SMA
  • •Review and approve abstracts and manuscripts
  • •Support market access dossiers and benefit assessments
  • •Maintain relationships with academics and professionals
  • •Supervise patient-centric clinical study development
  • •Execute clinical studies aligned with brand plans
  • •Improve educational and training content
  • •Manage budgets for assigned projects
  • •Support country clinical trial enrollment

Languages

German – Business Fluent

English – Business Fluent

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