Global Medical Director, Riliprubart

Role Summary

Global Medical Director, Riliprubart based in Cambridge, MA. Lead medical strategy and execution for riliprubart across the product value chain, driving scientific insights and medical education to address unmet needs in neurology and related fields.

Responsibilities

• Co-develop, plan and lead the execution of the medical strategy for riliprubart across the product value chain.
• Co-create the IEGP strategy with Medical Evidence Generation Lead and other evidence generation-related functions: CSU, RWE, HEVA, MO&E and country teams.
• Lead the execution of assigned medical affairs studies (EAP). Provide input in design, monitoring, analysis, and communication of the assigned studies. Serve as a global medical point of contact for such studies for internal and external stakeholders.
• Contribute to insight generation plan and input to the assigned assets overall medical strategy.
• Provide strategic input to Scientific Communications team to plan and execute evidence dissemination and medical education plans.
• Build trust with Global external stakeholders to advance their understanding of the therapeutic area and evolve the treatment landscapes for CIDP and riliprubart.
• Oversee the design of medical programs/initiatives to drive the therapeutic value of riliprubart and address unmet medical needs (MAPs, PSP, Diagnostic support programs, CSRs, etc).
• Oversee adherence to allocated budgets, plan and execute activities aligned with strategy and cross-functional alignment.
• Accountable for medical affairs review and scientific integrity of internal and external medical materials.

Qualifications

• Deep expertise in Neurology & Neuromuscular Diseases, preferred.
• Minimum of 4 years’ experience in relevant Medical Affairs.
• Experience in strategic medical affairs or clinical development roles including KOL engagement, evidence generation and scientific communication at Global and Key Market level, preferred.
• Broad drug development experience with knowledge of regulatory, market access and reimbursement.
• Experience managing clinical trials in a pharmaceutical environment strongly desired.
• Specialty care product launch experience at a country level, strongly preferred.
• Significant line and matrix management experience with collaboration across Research, Clinical Development, Commercial, Health Economics, Value & Access, and Product Management.

Skills

• Strategic thinking and ability to disrupt with innovation while remaining pragmatic.
• Result orientation and ability to develop and execute strategy, manage ambiguity, and take calculated risks.
• People leadership with talent development, feedback, coaching, and collaboration.
• Stakeholder management and collaboration across functions.
• High ethical, regulatory and scientific standards.

Education

• Doctorate in a relevant scientific discipline or Pharmacy; Medical Degree preferred.
• Languages: English (fluent).