Senior Manager, Digital Enablement

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.

• Lead scoping, requirements gathering, and business case for digital initiatives in Development
• Drive and maintain the digital roadmap within the domain, ensuring alignment with strategic goals and business priorities
• Collaborate with internal and external providers to ensure digital solutions run efficiently, remain compliant, and that issues are resolved promptly
• Support daily operation and maintenance of digital solutions within the domain, ensuring oversight of issues and system efficiencies
• Represent business areas during execution and delivery of digital solution projects
• Contribute to process design for new digital initiatives
• Evaluate delivered projects, measure benefits, and identify opportunities to enhance existing solutions

• Bachelor's degree in Life Sciences, IT, Engineering, or a related field
• 5-8 years of pharmaceutical or biotech experience, including at least 5 years in a similar role or as a system manager for digital solutions within Clinical Development (e.g., Veeva)
• Proven expertise in daily operations and maintenance of enterprise IT platforms such as Veeva Vaults, or other IT systems in clinical development
• Experience collaborating with Clinical Development, Regulatory Affairs, Quality Assurance, or similar domains is an advantage
• Strong background in IT compliance and Computer System Validation (CSV) requirements (e.g., GAMP, IT testing, validation)
• Proven track record in IT projects as a Subject Matter Expert, Senior Functional Lead, or Senior Project Manager
• Excellent written and verbal English communication skills, with the ability to convey complex concepts to both technical and non-technical stakeholders

• 401(k) Plan: 100% match on the first 6% of contributions
• Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
• Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
• Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
• Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
• Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

• 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!