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

The Programming Manager will contribute to the development, validation, maintenance, and lifecycle management of technology solutions and standards used across Clinical & Statistical Programming. 

 This role may serve as the owner for one of our existing pillars of focus and/or contribute to individual initiatives as a subject matter expert. 

Pillars include: 

• Statistical Computing Environment 
• R/Open-Source 
• Analysis Data Standards 
• Reporting Standards and Utilities 

Key Responsibilities: 

• Shape and execute the technology roadmap, enabling the adoption of new tools, processes, and integrations to enhance the clinical & statistical programming function and accelerate trial delivery. 
• Collaborate with cross-functional stakeholders (e.g. Biostatisics, Data Management, Medical Writing, IT) to gather requirements for standards and tools used to deliver clinical trial analyses. 
• Develop, validate, and maintain reusable standard code, macros, and packages using SAS and/or R. 
• May support operational activities within the Statistical Computing Environment (SCE), including troubleshooting, maintenance, and user support. 
• Ensure adherence to regulatory requirements (e.g., 21 CFR Part 11) and maintain audit-ready documentation for GxP-compliant systems 

Requirements 

• Minimum Bachelor’s degree.
• At least 5 years of experience within the pharmaceutical or Biotech industry programming. 
• Hands-on support of GxP-compliant system(s).   
• Experience in process development and/or improvement initiatives.   
• Practical knowledge of regulatory compliance requirements for GxP computer systems.  
• Familiarity with open-source development practices, tools, and industry trends  
• Experience in technology evaluation and vendor tools integration. 
• Programming languages: Required – Proficiency and hands on experience in SAS, (including macro programing) & R.  Python, Power Fx a plus.
• Proficient in both written and spoken English. 
• Experience working in a global context is preferred 

**Active contributor to industry-focused open-source communities (i.e. R in Pharma, Phuse-Pharmaverse), highly desired** 

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.

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