The Associate Director, Global Talent Management at Genmab will lead global initiatives in Leadership Development and Performance Management. Responsibilities include designing impactful leadership programs, improving performance management processes, and aligning talent management with R&D needs while fostering company culture and collaborating with diverse teams.

The Finance Manager will oversee financial operations, manage budgeting and forecasting, ensure compliance with standards, enhance financial strategies in alignment with global objectives, and lead various projects in a dynamic team environment.

The Vice President, Head of QA will lead the global Quality Assurance team, ensuring compliance with quality standards and GxP regulations. This role involves developing the QA organization, managing resources, and effectively communicating QA results to upper management. It requires oversight of GxP inspections and improvement of the Quality Management System, contributing to Genmab's mission of innovative cancer treatments.

The Manager, Internal Audit at Genmab will enhance internal audit processes through data analytics and AI. Key responsibilities include supporting SOX compliance, conducting audits, developing data-driven tools, and collaborating with the IA team on operational efficiency. The role requires strong data analysis expertise and relevant compliance knowledge.

Lead target identification and validation for antibody-based therapies, ensuring integration of computational and experimental biology approaches. Oversee a team of scientists, manage collaborations, and develop strategic direction for drug discovery efforts.

The Director of Thought Leader Engagement at Genmab is responsible for engaging with Key Opinion Leaders in Hematology/Oncology, driving advocacy and insights to inform brand strategy. The role involves developing engagement strategies, managing relationships with KOLs and MEs, executing plans at congresses, and working closely with marketing and sales teams to meet business goals.

The Senior Manager, Global Supply Chain Serialization at Genmab will oversee compliance with serialization regulations, manage serialization systems, enhance workflows in packaging and supply chains, and collaborate with teams to resolve serialization issues while ensuring high-quality pharmaceutical deliveries.

The Associate Director will shape and execute key marketing strategies for Genmab’s product EPKINLY, collaborating with various teams to drive brand growth, engage customers, and leverage innovative technologies.

The Associate Director/Director of Indirect Tax at Genmab will manage VAT and customs matters, providing advice across European entities, collaborating with stakeholders, ensuring compliance with indirect tax laws, and optimizing processes. The role requires a strong understanding of indirect tax dynamics and excellent communication skills.

The Senior Manager or Manager, GMP QA (GQP QA) at Genmab will oversee GQP operations, collaborate with subcontractors on quality matters, and establish the Marketing QA Department. The role requires a strong background in pharmaceutical QA, effective communication, and teamwork to drive improvements and ensure compliance with quality standards.

The Payroll Operations Specialist will manage payroll operations, ensuring compliance with Dutch labor laws and collaborating on HR projects to enhance departmental efficiency. Responsibilities include executing payroll processes and being a primary contact for payroll matters for local and remote employees across multiple countries.

As a Senior CMC Specialist in Downstream Processing, you will develop strategies and oversee lifecycle management of biopharmaceutical products, ensuring compliance with regulatory standards. Responsibilities include managing DSP activities in collaboration with CMOs and preparing necessary technical and regulatory documentation.

As a Senior Analytical CMC Specialist, you will lead analytical strategies for late-stage development of antibody therapies, oversee CMOs' analytical activities, prepare technical documents, and support CMC regulatory submissions. You will collaborate with various project teams and specialists to refine analytical processes and strategies.

The Sr. Manager or Manager of Safety Operations & Data Management is responsible for overseeing all safety data management and case processing activities related to pharmacovigilance for both developmental and post-marketing phases. This includes regulatory compliance, case assessments, managing vendor relationships, and contributing to safety systems implementation.

The Senior Director, Strategic Planning & Effectiveness will drive strategic business planning and cross-functional communication for Genmab in the U.S. market. This role involves overseeing resource tracking, preparing high-level materials, implementing process improvements, and collaborating with various teams to ensure alignment and efficiency in operations.

The Associate Director will be responsible for managing clinical vendor relationships, coordinating sourcing for new trials, and overseeing the escalation of issues. They will drive outsourcing processes, manage service agreements, and collaborate with internal and external stakeholders to ensure efficient trial operations.

The Associate Director of Biostatistics at Genmab acts as a statistical expert, leading clinical development strategies and providing input on trial design and regulatory submissions. Responsibilities include overseeing statistical methods across trials, advising on innovative methodologies, engaging with regulatory authorities, and ensuring the quality and consistency of data handling.

The Senior Manager, FP&A at Genmab will oversee financial planning, analysis, and controlling for Corporate and Enabling functions. Responsibilities include budget preparation, forecasting, reporting, and the implementation of new financial systems. This role will involve collaboration with global teams to support financial insights and adherence to financial procedures.

The Director will develop and execute global market access and pricing strategies for oncology assets, ensuring value demonstration to HTA bodies and payers. Responsibilities include connecting with cross-functional teams, supporting evidence generation, analyzing market trends, and optimizing launch strategies for successful patient access.

The Senior Manager, QA GMP Commercial & Lifecycle at Genmab oversees compliance with regulations and industry standards in commercial manufacturing activities. Responsibilities include quality oversight of contract manufacturing organizations, batch review, maintaining the Pharmaceutical Quality System, and handling deviations and CAPAs. This role also involves providing GMP training and collaborating with project teams.