The Associate Director, Key Customer Strategy will develop and execute strategies for EPKINLY, driving brand growth through cross-functional collaboration and leadership in oncology marketing.

The Senior Manager, Global Supply Chain Serialization will oversee serialization compliance, manage serialization systems, enhance workflows, and ensure quality pharmaceutical products to patients.

As a Senior Manager/Manager in GMP QA, you will oversee GQP operations, collaborate with subcontractors and Global QA, and establish a Marketing QA Department for antibody drugs.

The role involves managing VAT and customs related matters, providing indirect tax advice, and collaborating with various stakeholders to ensure compliance with indirect tax laws.

The Senior CMC Analytical Specialist oversees analytical strategies for late-stage antibody development, ensures compliance, and collaborates with project teams to support regulatory submissions.

The role involves managing case processing and safety data management in pharmacovigilance, ensuring compliance with regulations, oversight of CRO activities, and maintaining safety systems.

Manage payroll operations ensuring compliance with Dutch labor laws, collaborate on HR projects, and enhance department efficiency.

The Senior CMC Specialist will manage late-stage Downstream Processing activities, ensuring regulatory compliance and overseeing process characterization at partnered CMOs. Responsibilities include developing strategies, troubleshooting, and preparing CMC submission documents.

The Senior Director, Strategic Planning & Effectiveness will drive business strategies, oversee operations, and manage cross-functional communication in the U.S. oncology market.

The Associate Director will manage vendor relationships for clinical trials, coordinate sourcing for trials, and oversee vendor contracts and governance processes.

The Senior Manager, FP&A is responsible for global financial planning, analysis, and controlling across multiple functions, providing financial support and insights to the business, and facilitating budgeting and forecasting processes.

The Associate Director, Biostatistics provides statistical expertise in clinical development and regulatory submissions, guiding strategies and analyses while overseeing multiple projects.

The Director will develop global market access and pricing strategies for oncology products, collaborating with cross-functional teams to maximize asset value and ensure optimal patient access.

The Senior Manager will oversee QA GMP activities, ensure compliance with regulations, manage contract manufacturing organizations, and improve quality systems.

The Associate Director will support strategic capital allocation, lead financial modeling and valuation analyses, and collaborate across various functions to enhance business strategies and decision-making.

The Director of Marketing Operations oversees the US Sales & Marketing teams' operations, managing processes, vendor relations, and project execution, while providing strategic insights for efficiency improvements.

Manage the incentive compensation process for field teams, ensuring effective design and implementation while coordinating with various departments. Oversee operations, reporting, and quality assurance, aiming for optimal performance aligned with industry benchmarks.

The Senior CMC Stability Associate will manage stability activities, oversee outsourced testing and ensure compliance with quality standards for biologics development.

Manage commercial programs, oversee manufacturing activities, coordinate with external partners and health authorities, and maintain project quality in collaboration with various teams.

The Director will develop and maintain Genmab's Global Data Privacy Program, focusing on privacy engineering strategies and third-party risk compliance. The role requires collaboration with cross-functional teams to ensure adherence to data privacy regulations and to implement technical solutions.