Director, Patient Experience & Regulatory Strategy

Alexion Pharmaceuticals, Inc.; Boston (MA); Presencial; USD 152.000 - 228.000; Jornada completa

Descripción de la vacante

Alexion Pharmaceuticals, Inc. seeks a Senior Patient Experience and Regulatory Engagement professional in Boston to lead the integration of patient experience data (PED) into regulatory interactions across Global Medical Affairs, R&D, and Marketing & Market Access.

You will synthesize patient preference studies, lived-experience data, and PROs to shape risk/benefit narratives and prepare for key meetings with regulators and payors. Domestic and international travel (20-30%) is required.

Formación

• Bachelor’s degree in data science or management preferred.
• 10+ years in Biotech/Pharma with regulatory or clinical development experience.
• Ability to translate regulatory shifts into PED data strategies.
• Experience generating or synthesizing patient experience data for regulatory submissions.
• Willingness to leverage AI and emerging technologies.
• Ability to lead complex global initiatives in a matrix organization.

Responsabilidades

• Lead cross-functional strategy to integrate PED into regulatory submissions.
• Translate regulatory landscape shifts into PED data generation strategies.
• Provide leadership to generate PED including patient preference and lived-experience evidence.
• Lead vendor partnerships with clear scope and timely outputs.
• Travel domestically and internationally 20-30%.

Conocimientos

Leadership

Regulatory knowledge

Patient-focused data

Strategic thinking

Communication skills

Cross-functional collaboration

AI familiarity

Educación

Bachelor’s degree in data science or management

Advanced degree (MPH, MBA, MPA, PhD, MD)

Descripción del empleo

Alexion Pharmaceuticals, Inc. seeks a Senior Patient Experience and Regulatory Engagement professional in Boston to lead the integration of patient experience data (PED) into regulatory interactions across Global Medical Affairs, R&D, and Marketing & Market Access.

You will synthesize patient preference studies, lived-experience data, and PROs to shape risk/benefit narratives and prepare for key meetings with regulators and payors. Domestic and international travel (20-30%) is required.