Associate Director, Programming Open Source

Genmab • Lincoln, NE

6d • $164,080 - $246,120

About The Position

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! Associate Director – Open Source The Associate Director – Open Source is a technical leader within the Programming Standards and Technology organization who drives the implementation and governed adoption of open-source technologies in a GxP-compliant environment. This role exists at the intersection of process, standards, and technology, providing deep technical mentorship, resolving complex issues, and ensuring seamless integration of open-source solutions into existing workflows. The Associate Director partners with governance bodies, contributes to enterprise strategy, and maintains strong industry awareness to advance programming innovation and excellence.

Requirements

• 10+ years of relevant experience in the Pharmaceutical/Biotech Industry.
• Bachelor’s or Master’s degree in statistics, biostatistics, computer science, or a related field.
• Skilled statistical programmer with strong knowledge of CDISC data models, efficient coding practices, and contextual understanding of clinical data.
• Advanced R programming skills, including familiarity with Pharmaverse; Python experience a plus.
• Practical knowledge of open-source package validation, repository management, and reproducible environment strategies.
• Well-versed in industry best practices related to the application of package-based open-source software in GxP-compliant environments.
• Knowledge and experience leading the development of dynamic, reusable code.
• Practical experience applying SDLC to the development, maintenance, and validation of standard code and/or business applications.
• Analytical, thorough, and proactive, with the ability to manage multiple tasks independently while maintaining high quality and accountability.

Nice To Haves

• Active participation in industry organizations (e.g. PHUSE, R Consortium, R in Pharma), including contributing to working groups or standards discussions, a plus.

Responsibilities

• Own one or more enterprise capabilities within Programming Standards and Technology from concept to global rollout—defining roadmap, architecture, and implementation strategy, including change management.
• Implement Genmab’s open-source strategy for clinical and statistical programming, leading process and training to drive the adoption of new technology components.
• Accountable for driving execution of project-based initiatives and operational goals, ensuring solutions are aligned with internal business needs, external requirements, and industry best practices.
• Collaborate with the Programming Leadership Team (LT) and standards governance forums to identify priorities, pilot opportunities, and monitor adoption of capabilities.
• Provide technical direction and mentorship to supporting subject matter experts (SMEs), resolving complex programming or implementation challenges.
• Represent Statistical Programming in cross-functional governance and decision-making forums to maintain visibility and alignment with partner functions (i.e. Biostatistics, Data Management, IT, QA).
• Continuously improve processes, standards, and technology by staying abreast of evolving global regulatory requirements and industry trends.
• Oversee regulatory compliance (e.g., 21 CFR Part 11) through effective governance, ensuring systems and documentation remain audit-ready for GxP operations.
• Provide strategic support for cross-pillar projects and operational initiatives across the Process, Standards, and Technology portfolio.
• Drive requirements for enterprise business platforms to ensure interoperability with established open-source capabilities and extensibility to meet future needs.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Director