Leads EMEA learning strategy and programs across clinical, commercial, and leadership capabilities, aligning global standards with local needs while ensuring compliant training, certification, and measurable impact.
Build and lead enterprise data capabilities by connecting business systems, delivering trusted analytics, and establishing scalable architecture, governance, and AI foundations across the organization.
Leads global evidence-generation strategy and execution for commercial and pipeline therapies, producing clinical, economic, and patient-centered evidence to demonstrate value and inform access and healthcare decisions.
Leads Medical Affairs operations by aligning strategy, budgets, governance, research, compliance, and executive communications to support cross-functional execution and scalable global operations.
Leads EMEA patient advocacy and communications, building trusted community partnerships and translating patient insights into strategy while shaping corporate reputation, executive visibility, and regional communications.
Leads external and CMC quality assurance for biologics, overseeing contract partners, quality systems, product disposition, and inspection readiness while managing quality risks across clinical and commercial product lifecycles.
Lead non-U.S. indirect tax strategy, compliance, technology, and controversy, serving as the subject matter expert for VAT, GST, and related transaction taxes while partnering across Finance, Supply Chain, and Legal.
Lead U.S. domestic tax accounting, compliance, planning, and controversy, owning tax provision and federal and multistate filings while advising on business transactions and driving tax work for an ERP implementation.
Manage EMEA accounting across multiple entities, coordinating monthly close, revenue and OPEX reporting, Gross-to-Net processes, reconciliations, and SOX controls while improving accounting procedures.
Lead market insights and competitive intelligence for a newly launched neuromuscular treatment, translating research and market dynamics into evidence-based commercial strategies and launch optimization.
Lead clinical development strategy for assigned pipeline products, oversee trial safety and medical monitoring, and guide study design, regulatory responses, and interpretation of clinical data across cross-functional teams.
Leads statistical activities across clinical studies from design through regulatory submission, developing analyses, interpreting results, and guiding clinical development decisions in rare disease programs.
Leads device engineering strategy and hands-on development for biologic combination products, including prefilled syringes and autoinjectors, from drug-device integration through validation, regulatory support, and lifecycle management.
Develop regulatory strategy for clinical and pipeline programs, guide agency engagement, lead regulatory interactions and submissions, and advise cross-functional teams on risks, opportunities, and compliance.
Provides technical leadership for monoclonal antibody downstream manufacturing across external partners, supporting GMP production, technology transfer, process validation, monitoring, investigations, and commercial lifecycle management.
The Senior Accountant will support the monthly close process, maintain financial records, and ensure scalable accounting processes while collaborating with the Accounting team on various reporting and compliance tasks.
The Associate Director/Director of Clinical Operations Compliance will oversee adherence to standard procedures, support issue management, and ensure clinical programs are inspection ready.
The Vice President, Head of Regulatory Strategy will build and lead global regulatory strategy across the portfolio, guide program teams, and direct agency engagement and regulatory submissions.
Leads drug safety strategy and pharmacovigilance across product development and lifecycle, evaluating safety data, managing signals and risks, and guiding cross-functional teams on regulatory and clinical safety matters.
Coordinates personalized education and care for patients with SMA, guiding patients and caregivers through therapy access, affordability, and logistics while partnering with healthcare teams to address non-clinical barriers.
Coordinate personalized education and non-clinical access support for patients with spinal muscular atrophy, serving as their advocate and connecting patients, caregivers, healthcare teams, and support resources throughout treatment.
Guide patients and caregivers through SMA treatment by providing personalized education, coordinating therapy access and logistics, and connecting them with healthcare teams and support resources.
Develops SMA accounts and market demand by educating healthcare providers, identifying patients, coordinating access and treatment logistics, and aligning stakeholders to support treatment decisions and sales goals.
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