Jobs at Eisai US

Leads quantitative systems pharmacology strategy and develops mechanistic mathematical models supporting drug discovery, clinical development, dose selection, efficacy and safety assessment, and translational decisions. Applies computational, statistical, and biological expertise across neurology, oncology, and other therapeutic areas; guides QSP platform development, advances model-informed drug development, collaborates across teams, presents scientific findings, and manages modeling deliverables.

Leads market access and account management training strategy for pharmaceutical commercial teams across neurology and oncology. Develops e-learning, workshops, assessments, classroom and experiential training; facilitates train-the-trainer programs; ensures regulatory review; manages budgets, vendors, stakeholders, direct reports, mentoring and team development. Requires pharmaceutical industry expertise, market access and reimbursement knowledge, account management experience, therapeutic-area familiarity, presentation skills, and virtual training design experience.

Lead development, review, approval, and maintenance of Company Core Data Sheets (CCDS), Country Product Information (CPI) and related components. Coordinate cross-functional teams, provide regulatory labeling strategy and tactical guidance, manage direct reports, ensure SPL compliance for US submissions, maintain labeling history, and support global labeling intelligence and special GRN/GL initiatives.

Lead global regulatory labeling strategy and operations for neurology and oncology products. Oversee development and maintenance of CCDS, USPI, EU SmPC and country labels, manage labeling teams, EDMS repositories and workflows, ensure regulatory compliance and consistency, and liaise with partners and stakeholders.