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Senior Programming Manager
Genmab • Princeton, TX1d • Hybrid
Sas Programmer Jobs
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Senior Programming Manager
Genmab•Princeton, TX
•Hybrid
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! The Senior Programming Manager leads programming activities for complex or multiple trials, ensuring consistency and excellence across deliverables. This role contributes to enterprise-level standards, training, and capability building, and oversees programming in support of regulatory submissions. As a subject matter expert in CDISC standards, regulatory requirements, and/or systems/process innovation, the Senior Programming Manager shapes proposals for governance and supports strategic initiatives that advance programming practices globally.
Requirements
- Bachelor’s or Master’s degree in statistics, biostatistics, computer science, or a related field and/or 8+ years of relevant experience in pharmaceutical/biotech environments.
- Skilled SAS programmer with strong knowledge of CDISC SDTM/ADaM models, efficient coding practices, and contextual understanding of clinical data.
- Analytical, thorough, and proactive, with the ability to manage multiple tasks independently while maintaining high quality and accountability.
- Collaborative team player with excellent communication, planning, and knowledge-sharing abilities.
Nice To Haves
- Oncology submission experience preferred
Responsibilities
- Provide hands-on leadership for a trial of high complexity or multiple trials
- Drive consistency across trials.
- Contribute to enterprise standards and/or training; act as CDISC/regulatory SME.
- Support major Standards/Systems/Process capability, shaping proposals for the governance board.
- May oversee all programming activities in support of regulatory submission.
- Act as SME and/or pillar owner in the capability-governance framework.
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
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What This Job Offers
Job Type
Full-time
Career Level
Senior
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Based on current job postings on Teal, the average Sas Programmer salary in the US is approximately $124,000 per year, with a typical range of $87,000 to $170,000.
