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Genmab

Senior Programming Manager

Genmab · United States

  • Hybrid
  • Full-time
  • $150,000 / year
  • United States

Job highlights

  • Lead complex programming for clinical trials.
  • Ensure data consistency and regulatory compliance.
  • Contribute to enterprise standards and training.
  • Expertise in SAS and CDISC standards required.
  • Drive innovation in programming practices globally.

About the role

Senior Programming Manager

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 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

  • 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.
  • Oncology submission experience preferred

Compensation and Benefits

For US based candidates, the proposed salary band for this position is as follows: $128,080.00---$192,120.00. The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

When You Join Genmab, You’re Joining a Culture That Supports Your Physical, Financial, Social, And Emotional Wellness. Within The First Year, Regular Full-time U.S. Employees Are Eligible For:

  • 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

About You

  • 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!

Locations

Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate.

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X.

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com).

Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.

Key skills/competency

  • SAS Programming
  • CDISC Standards (SDTM/ADaM)
  • Clinical Data Analysis
  • Regulatory Submissions
  • Biostatistics
  • Data Management
  • Pharmaceutical Industry
  • Team Leadership
  • Project Management
  • Problem Solving

Skills & topics

  • Senior Programming Manager
  • SAS Programming
  • CDISC
  • SDTM
  • ADaM
  • Clinical Data
  • Biostatistics
  • Oncology
  • Regulatory Submission
  • Biotechnology
  • Pharmaceutical
  • Data Analysis
  • Programming Lead
  • Clinical Trials
  • Genmab

How to get hired

  • Tailor your resume: Highlight SAS programming, CDISC standards, and oncology submission experience.
  • Craft a strong cover letter: Emphasize your passion for Genmab's mission and your leadership skills.
  • Prepare for technical interviews: Be ready to discuss SAS coding, SDTM/ADaM, and clinical data.
  • Showcase your collaboration: Demonstrate your ability to work effectively in a team and share knowledge.
  • Research Genmab's culture: Align your answers with their values of compassion, purpose, and scientific innovation.

Technical preparation

Master SAS programming, including macro programming.,Deeply understand CDISC SDTM and ADaM standards.,Practice writing efficient and compliant clinical code.,Familiarize yourself with clinical data structures.

Behavioral questions

Describe a complex programming challenge you solved.,How do you ensure data quality and consistency?,How do you collaborate with cross-functional teams?,Share an example of driving process innovation.

Frequently asked questions

What are the key technical skills required for the Senior Programming Manager role at Genmab?
The Senior Programming Manager role at Genmab requires strong SAS programming skills, a deep understanding of CDISC SDTM/ADaM models, and efficient coding practices. A contextual understanding of clinical data is also essential, along with experience in the pharmaceutical or biotech environments. Oncology submission experience is preferred.
What is the typical career progression for a Senior Programming Manager at Genmab?
While specific paths may vary, a Senior Programming Manager at Genmab can progress into more senior leadership roles, potentially managing larger teams or broader programming initiatives. They may also become subject matter experts, influencing enterprise-level standards and strategic direction for programming practices globally.
What kind of clinical trials would a Senior Programming Manager at Genmab typically work on?
A Senior Programming Manager at Genmab would likely lead programming activities for complex or multiple clinical trials. Given Genmab's focus, these trials would primarily be in the area of oncology, developing antibody therapeutics and medicines to treat cancer and other serious diseases.
How does Genmab support the professional development of its Senior Programming Managers?
Genmab invests in employee growth through various means. The Senior Programming Manager role itself offers opportunities to contribute to enterprise standards, training, and capability building. The company also provides resources like tuition reimbursement and a supportive culture that encourages innovation and knowledge sharing, fostering continuous learning.
What is Genmab's approach to remote work for roles like the Senior Programming Manager?
Genmab aims to maximize the efficiency of an agile working environment for employee work-life balance. While specific arrangements can vary, the company culture supports connection whether employees are in office spaces or working remotely, emphasizing collaboration and innovation across all settings.