Description

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 Role

The Senior Manager, Commercialization Operations & Business Effectiveness (CO&BE) is a key integrator of all Commercialization activities for a given brand/asset, with a focus on enabling coordinated execution and scalability across launches. The Senior Manager is accountable for Commercialization Project leadership and will work closely with cross functional colleagues to drive innovation and operational excellence within the critical business areas of: Launch Readiness, Executive Leadership Support, Strategic & Tactical Planning, Governance, and Continuous Improvement.

Work arrangement: This role offers flexibility to work away from the office for 20%-40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60-day period, and is approved by the hiring manager.

This role reports directly to the Director, CO&BE.

Responsibilities

• Manages Commercialization Projects as a core member of the Launch Team, enabling scalable launch execution and market readiness.
  
• In partnership with the Director, coordinates development and execution of cross-functional readiness plans.
  
• Coordinates day-to-day activities across cross-functional teams (e.g., Market Access, Medical, Commercial, Regulatory) to ensure aligned execution toward shared outcomes.
  
• Supports market-level launch readiness, coordinating key components to enable successful launch readiness.
  
• Coordinates launch readiness activities, governance processes, and continuous improvement efforts, supporting delivery of key project outputs and effectively leveraging cross-functional teams and vendor partnerships.
  
• Responsible for maintaining integrated project plans, proactively tracking risks, dependencies, and trade-offs across markets to support successful delivery.
  
• Partners with stakeholders to align timelines and reporting with global milestones and market-specific requirements (e.g., regulatory, access, and launch sequencing), proactively identifying risks and interdependencies.
  
• Supports development of clear project plans and materials, ensuring appropriate visibility across global, regional, and local stakeholders to enable alignment and informed decision-making.
  
• Coordinates clear, consistent communication across global, regional, and local stakeholders, tailoring messaging to different levels of the organization.
  
• Supports preparation of materials and inputs for governance forums, ensuring decisions are informed by clear insights, trade-offs, and cross-functional perspectives.
  
• Maintains project information, documentation, and team communications to ensure timely and accurate visibility of project status for governance bodies and key stakeholders.
  
• Fosters and contributes to a high-performing team environment, supporting strong team dynamics and effective collaboration.
  

Requirements

• BA/BS required plus 5 years' experience; MBA plus 3 years' experience or other related advanced degree strongly preferred.
  
• 3-5 years of experience as a project manager in a pharmaceutical/biotech company including process improvement or change initiatives.
  
• Oncology/Hematology experience is required.
  
• Experience in market approval and/or commercial launch phases is required.
  
• Proven experience in oncology product launches, with strong understanding of market access dynamics, regulatory requirements, and cross-market launch sequencing.
  
• Proven ability to manage multiple complex, interdependent projects simultaneously, driving timelines, budgets, and proactively resolving cross-team issues, while maintaining alignment to long-term strategy.
  
• Project leadership and strong organizational skills are required.
  
• Strong business acumen with the ability to synthesize complex information into clear insights, recommendations, and decision frameworks for stakeholders.
  
• Demonstrated ability to influence without authority, effectively driving alignment and results across global and market teams.
  
• Experience preparing materials and insights for governance forums and supporting senior leadership decision-making.
  

About You:

• You are well-organized and have a structured mindset.
  
• You communicate clearly, effectively, and respectfully with colleagues across different roles, levels, and areas of the organization.
  
• You are detail orientated with a marked ability to see the bigger picture.
  
• You are proactive in identifying improvements and efficiencies and able to communicate with your stakeholders across the organization and business areas.
  
• You have a global mindset and the ability to partner cross-culturally.
  
• You are resilient, determined, accurate and deliver as committed.
  
• You have demonstrated ability to resolve conflict and influence teams without formal authority.
  
• You can synthesize parallel requests and timelines to prioritize requirements, functions, and features for greatest customer value.
  
• You demonstrate intellectual curiosity.
  
• You thrive in a dynamic setting, handling multiple concurrent tasks.
  

For US based candidates, the proposed salary band for this position is as follows:

$133,600.00---$200,400.00

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.