Senior Programming Manager
Genmab
June 27, 2026
Remote friendly (United States)
United States
Clinical Research and Development
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.
Senior Programming Manager Role
- 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
Experience/Qualifications
- Bachelor’s or Master’s degree in statistics, biostatistics, computer science, or related field and/or 8+ years relevant experience in pharmaceutical/biotech environments
- SAS programming with strong knowledge of CDISC SDTM/ADaM models, efficient coding practices, and contextual understanding of clinical data
- Analytical, thorough, proactive; manage multiple tasks independently with high quality and accountability
- Collaborative; excellent communication, planning, and knowledge-sharing abilities
- Oncology submission experience preferred
Benefits (U.S. based candidates, within first year for regular full-time employees)
- 401(k): 100% match on first 6% of contributions
- Health benefits (two medical options including HDHP with HSA), dental, and vision
- Voluntary plans: critical illness, accident, hospital indemnity
- Time off: paid vacation, sick leave, holidays, and 12 weeks discretionary paid parental leave
- Support resources and additional perks: commuter benefits, tuition reimbursement, Lifestyle Spending Account
Proposed salary band (U.S.): $128,080.00–$192,120.00
Senior Programming Manager Role
- 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
Experience/Qualifications
- Bachelor’s or Master’s degree in statistics, biostatistics, computer science, or related field and/or 8+ years relevant experience in pharmaceutical/biotech environments
- SAS programming with strong knowledge of CDISC SDTM/ADaM models, efficient coding practices, and contextual understanding of clinical data
- Analytical, thorough, proactive; manage multiple tasks independently with high quality and accountability
- Collaborative; excellent communication, planning, and knowledge-sharing abilities
- Oncology submission experience preferred
Benefits (U.S. based candidates, within first year for regular full-time employees)
- 401(k): 100% match on first 6% of contributions
- Health benefits (two medical options including HDHP with HSA), dental, and vision
- Voluntary plans: critical illness, accident, hospital indemnity
- Time off: paid vacation, sick leave, holidays, and 12 weeks discretionary paid parental leave
- Support resources and additional perks: commuter benefits, tuition reimbursement, Lifestyle Spending Account
Proposed salary band (U.S.): $128,080.00–$192,120.00