At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! The role Genmab is seeking a motivated individual to join a team committed to delivering quality submissions. A Senior Manager is responsible for activities related to regulatory publishing and submission management support to FDA, EMA, MHRA, SwissMedic and more. Seeks to contribute into innovation process while supporting GRA strategy and deliverables. Supports activities to implement new technology solutions in support of regulatory publishing business process. Responsibilities Responsible for the creation, assembly, and publishing of both major and routine global electronic submissions (eCTD and NeeS), including MAA, BLAs and INDs for Original Applications, DSURs, Supplements, and more. Serve as the global submissions' expert, guiding teams on e-submission standards (eCTD, NeeS, etc.) and lifecycle management, while clearly communicating regional regulatory differences. Perform QC and technical validation of electronic submissions to ensure compliance with internal standards and external criteria before delivery to the Regulatory Users for internal review/approval. Adherence to required submission timelines, health authority publishing specifications, and internal working practices. Liaise with functional source areas (clinical, nonclinical, regulatory) to ensure documents are compliant with authoring style guide. Work with regulatory document authors to achieve resolution and ensure that documents comply with regulatory and company guidance/template specifications. Maintain working knowledge of the regulations and processes that govern the content and maintenance of controlled documents required by the Health Authorities and ICH. Represent Regulatory Operations on project teams, driving timelines and deliverables related to submission documents. Requirements BA/BS degree or equivalent, at least 8 years pharmaceutical industry experience, and prior Regulatory Operations experience required. Knowledge of IND, BLA, MAA,regarding CTD requirements and guidelines, for both eCTD and NeeS. Knowledge of industry trends regarding electronic submissions. Technical knowledge of electronic publishing systems and software. Proficiency with MS-Office Suite and Adobe Acrobat application. Knowledge of health authority procedures/guidance's regarding electronic submissions. Knowledge of Electronic Document Management Systems. Ability to balance multiple tasks to meet priorities and timelines. Self-starter with superior time management skills, and ability to work independently or in teams. Strong attention to detail. Strong communication skills - both oral and written Nice to have submission management skills. About You You are genuinely passionate about our purpose You bring precision and excellence to all that you do You believe in our rooted-in-science approach to problem-solving You are a generous collaborator who can work in teams with a broad spectrum of backgrounds You take pride in enabling the best work of others on the team You can grapple with the unknown and be innovative You have experience working in a fast-growing, dynamic company (or a strong desire to) You work hard and are not afraid to have a little fun while you do so! Locations Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate. About Genmab Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X. Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com).

Senior Manager, Global Regulatory Operations, Publisher

Ready to interview?

Related listings