US Medical Director Neuromuscular

Role Summary

As US Medical Director, this person will be a strategic thought partner providing expert medical leadership and contributing to the development and execution of the US medical strategy. This person will lead content development, KOL education programs, and support our cross-functional field teams for the US. As a key member of the US Medical team, reporting to VP of US Medical Affairs, this person will be accountable for advancing SRK’s scientific leadership in Rare Neuromuscular Diseases including SMA and other pipeline indications. This person will thrive in this role if he/she is a self-starter and a highly collaborative individual who cares to have impact on patients in the rare disease space.

Responsibilities

• Strategic ownership of US Medical Plans – pre and post launch
• Organize external expert advisory boards, support scientific symposia, develop medical congress engagement strategy
• Act as medical lead for medical legal review committee (MLR)
• Analyze medical insights to inform cross-functional strategies and tactics
• Collaborate with cross-functional field teams to identify data and educational gaps
• Provide strategic input for the development of educational and messaging
• Lead the digital medical education strategy and execution
• Continuously raise the bar for our externally facing materials, ensuring alignment to strategy
• Oversee Medical activities related to review of promotional and scientific materials
• Collaborate with functional groups as subject matter expert including Patient Advocacy, Commercial Operations, New Products, and many other internal stakeholders in support of pipeline products
• Provide medical leadership to guide internal and external decision-making
• Establish and maintain strong knowledge in SMA to optimize clinical study protocols development and execution
• Establish and maintain strong relationships with experts in the field, academics and professionals
• Ensure a patient-centric approach to development of clinical studies under her/his supervision
• Collaborate cross functionally to execute the clinical studies under her/his responsibility in alignment with the Brand plan and Global Medical Plan
• Collaborate with Global Medical to identify and execute internally and externally sponsored studies
• Foster strong relationships with internal and external stakeholders to identify unique opportunities to improve and evolve educational and training content
• Manage budget for assigned projects

Qualifications

• Required: Minimum 5 years’ experience in industry R&D or Medical
• Required: Excellent written and communication skills, highly organized and able to manage multiple initiatives
• Preferred: MBA

Education

• MD, PharmD, PhD or equivalent scientific degree

Additional Requirements

• Travel required, comprising approximately 20%