Senior Programming Manager
Genmab
June 28, 2026
Remote friendly (Princeton, NJ)
United States
IT
Senior Programming Manager
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; shape 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.
Qualifications/Experience:
- Bachelor’s or Master’s degree in statistics, biostatistics, computer science, or 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, proactive; ability to manage multiple tasks independently with high quality and accountability.
- Collaborative team player with excellent communication, planning, and knowledge-sharing abilities.
- Oncology submission experience preferred.
Compensation/Benefits (US):
- Salary band: $128,080.00–$192,120.00.
- 401(k): 100% match on first 6% of contributions; medical/dental/vision; voluntary plans; paid time off incl. 12 weeks discretionary paid parental leave; backup care and wellness/emotional support; commuter benefits, tuition reimbursement, Lifestyle Spending Account.
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; shape 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.
Qualifications/Experience:
- Bachelor’s or Master’s degree in statistics, biostatistics, computer science, or 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, proactive; ability to manage multiple tasks independently with high quality and accountability.
- Collaborative team player with excellent communication, planning, and knowledge-sharing abilities.
- Oncology submission experience preferred.
Compensation/Benefits (US):
- Salary band: $128,080.00–$192,120.00.
- 401(k): 100% match on first 6% of contributions; medical/dental/vision; voluntary plans; paid time off incl. 12 weeks discretionary paid parental leave; backup care and wellness/emotional support; commuter benefits, tuition reimbursement, Lifestyle Spending Account.