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📑 The Role Genmab is now searching for a (Senior) Project Manager CMC to join the New Product Introduction (NPI) CMC Team in Copenhagen.The (NPI) CMC Team is part of CMC Operations in Copenhagen, which now has close to employees. CMC Operations is responsible for development and manufacture of Genmab antibody d ...

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📑 The Role & DepartmentThe Nonclinical Safety & Toxicology Team are looking for an experienced toxicologist for a newly created position as sponsor monitor for nonclinical safety studies with Genmab’s pharmaceutical drug candidates outsourced to our CRO laboratory partners.The Nonclinical Safety Team at Genmab ...

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📑 The Role & DepartmentGenmab is now searching for an experienced Senior Clinical Drug Supply Manager to be part of Global Clinical Drug Supply, CMC Operations and work according to Genmab's hybrid work arrangement in Princeton, NJ.ResponsibilitiesEstablishes ...

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📑 The Role & DepartmentThe quality area of Genmab is growing and looking for two student assistants. As Quality Assurance (QA) GMP student assistant you will work in a global ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & Department Genmab is on an exciting journey! In just a brief time, we have evolved from an R&D (Research & Development) company, who licensed its products for partners to market, to end-to-end biotechnology company with full commercialization capabilities and will shortly be bringing our products direc ...

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📑 The Role & DepartmentThe Associate Director, Standards & Systems is operationally responsible for the development, maintenance and adherence to Genmab’s clinical data standards including eCRFs, edit checks, controlled terminology, CDASH and SDTM mapping and etc. The role provides leadership for the continued development ...

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📑 The Role & DepartmentAs the Manager of Portfolio Planning, you will be in the Portfolio Management department and responsible for providing end-user support to drive analytics, resourcing, and program planning initiative. This would also include budgeting and reporting deliverables. In this highly collaborative role, you’ll b ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role The project portfolio at Genmab is evolving and we are therefore looking for an Associate Director to join the Regulatory Affairs CMC team.As Associate Director within Regulatory Affairs CMC at Genmab, you will be responsible for operational and strategic regulatory CMC input to support worldwide development and co ...

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📑 The Role & DepartmentGenmab is committed to transparency of clinical trial research. We recognize the scientific and ethical value of sharing clinical trial information in a non-biased and timely manner to benefit patients and other external stakeholders. The Clinical Trial Disclosure & Transparency (C ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role The Senior Statistical Manager supports the design, execution, analysis, interpretation, and reporting of clinical trials as well as communication of data evidence for Clinical Research & Development and Medical Affairs programs with minimal supervision. This position supports statistical aspects of ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & Department At Genmab we are now looking to further strengthen the Late Stage Development QA Team located in Denmark. In this position, the Quality Assurance (QA) Associate Director will set the quality direction for Genmab’s Late-Stage Development products.As GMP QA Associate Director you will be an ...

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📑 The Role & DepartmentIn Genmab’s expansive growth, we are now looking for a Senior Drug Product Subject Matter Expert (SME) to take upon the responsibility within the area of Compatibility and In-use for Genmab’s portfolio products. You will work closely together with early/late stage project teams as well as Drug Supp ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & DepartmentDo you want to join our highly talented Late-Stage Manufacturing Development (LSMD) Subject Matter Expert (SME) Team in CMC operation in Copenhagen, and be in direct contact with late phase development? With Genmab’s expansive growth, we work with great energy to prepare the CMC package for regulatory fil ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & DepartmentThe Senior Programming Associate / Programming Manager supports the development of new therapies by ensuring integrity, consistency, and adherence to standards of data and produces well-structured, high quality data summaries in tables, figures, and listings for decision making. ...

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📑 The Role :The Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early and late-stage programs, and/or as trial responsible statistician with responsibilities as described below. The Director contributes to clinical development strategies and plans. T ...

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📑 The Role & DepartmentGenmab is searching for an experienced Clinical Drug Supply Manager to be part of Global Clinical Drug Supply Operations in Copenhagen, DK or Princeton, NJ in commuting distance to our office locations to work according to our hybrid work arrangement.Moving forward ...

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📑 The Role & DepartmentAs the Senior Clinical Data Manager, you will be operationally responsible for tasks within the planning, start-up, conduct and closure of clinical trials from final synopsis and/or a Clinical Trial Team (CTT) is assigned.The Senior Clinical Data Manager will represent Clinical Operations Da ...

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📑 The Role & DepartmentAs a Senior Director, you will join our Global Regulatory Affairs organization. In this capacity, you will assume responsibility for the EU/ROW regulatory strategy for an assigned program and will manage a group of Regulatory Strategists with EU/ROW responsibilities for our programs across al ...

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📑 The Role & DepartmentAs the Contractor, Senior Clinical Data Manager, you will be operationally responsible for tasks within the planning, start-up, conduct and closure of clinical trials from final synopsis and/or a Clinical Trial Team (CTT) is assigned. The Contractor, Se ...

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📑 The Role :As an Associate Digital Product Manager in IT & Digital, you will have a critical role in overseeing the product strategy, development/implementation and management of technology products in different focus areas in Development Operations, including Trial Management, Trial Monitoring, Clinical Data Management, Trial ...

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📑 The Role At Genmab, AI and Digital Technologies are being developed, implemented, and utilized at a pace never seen before. Join Genmab as an Associate Director, Solution Architecture and En ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & DepartmentAs a Associate Director, Global Regulatory Affairs Project Lead you will be a part of our Global Regulatory Affairs organization. In this role, you will represent RA in the Clinical Trial Teams and work closely with the CRO and internal stakeholders to ensure ...

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📑 The Role The Director, Team Leader, External Data Quality Management, Clinical Data Management, at Genmab is operationally responsible for the oversight of External Data Quality Management activities related to effective planning and timely delivery of complete, high-quality, and reliable external data for clinical trials.< ...

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📑 The Role & DepartmentAs an (Associate) Director, Global Regulatory Affairs Project Lead you will join our Global Regulatory Affairs organization. In this capacity, you will assume responsibility for the EU/ROW regulatory strategy, closely collaborating with the Global Regulatory Team on one or multiple compounds in earl ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & DepartmentAs the Senior Clinical Data Manager, you will be operationally responsible for tasks within the planning, start-up, conduct and closure of clinical trials from final synopsis and/or a Clinical Trial Team (CTT) is assigned. The Senior Clinical Dat ...

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📑 The Role As a (Senior) Manager in External Data Acquisition, you will play a pivotal role within our Clinical Data Management team. Your primary responsibility will be to oversee the acquisition and integration of third-party data (e.g., laborat</sp ...

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📑 The Role & DepartmentGenmab is searching for an enthusiastic Senior Clinical Drug Supply Associate to be part of Global Clinical Drug Supply Operations in Copenhagen or Princeton within commute distance from our office locations to work according to your hybrid work arrangement.Having a ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & DepartmentGenmab is searching for an experienced and energized Associate Director to be part of Global Clinical Drug Supply Operations in Copenhagen or Princeton within commute distance from our office locations to work according to your hybrid work arrangement.Having an impr ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role Reporting to the Global Medical Affairs Strategy Lead (MASL), the Medical Director will be the subject matter expert responsible for providing medical support to the development and execution of the Global Medical Affairs strategic and tactical plans and support the Global medical launch planning, and execution for ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 The Role & Department As the inaugural leader of Genmab's clinical Inspection Readiness function, you will be instrumental in cultivating an international team committed to achieving superior inspection readiness </sp ...

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📑 The Role & Department The new laboratory facilities manager is based in Ballerup and supports Genmab’s innovative products by enabling release and stability testing according to ICH guidelines. You will have great impact on shaping working culture and laboratory capabilities meanwhile taking responsibility on yo ...

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📑 The Role We are looking to hire a new team member for our Development Strategic Sourcing Unit. The Senior Outsourcing Manager will drive, collaborate, and advise on the end-to-end contracting & outsourcing process for clinical trial services with external service providers within e.g., clinical drug supply, ...

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📑 The Role & Department Are you inspired to work in a company with ambitious goals, exciting clinical development programs, and highly enthusiastic colleagues? Our vision by is that Genmab’s knock-your-socks-off “KYSO” antibody medicines will transform the lives of people with cancer and other serious diseases. Do you want to ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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📑 At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our busine ...

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