Senior Project Manager, Late-Stage CMC Project Management

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!

At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.

About the Role

We are looking for a Senior Project Manager to drive complex projects in Genmab’s late-stage CMC project organization. You will translate project strategies into integrated plans and coordinate delivery across internal teams and contract development and manufacturing organizations (CDMOs).

Working within Genmab Tech Ops in Denmark, you will collaborate closely with colleagues across CMC, Regulatory Affairs, Quality and Supply Chain to advance late-stage programs towards regulatory submission and commercial readiness.

This role offers the opportunity to take ownership of project delivery, influence cross-functional decisions and strengthen project management practices through mentoring and continuous improvement.

Responsibilities

CMC project planning and delivery

• Develop and execute integrated project plans, timelines and milestones aligned with the Drug Development Plan. Provide input to optimize project strategy and translate agreed priorities into clear deliverables
• Coordinate internal and external activities, including technology transfer, process validation and manufacturing readiness, managing cross-functional dependencies and ensuring clear ownership and timely delivery
• Lead proactive risk management, prioritizing risks and driving mitigation, escalation and resolution. Maintain current plans, dashboards, action and decision logs, and communicate progress and emerging issues

Supplier coordination and regulatory readiness

• Create and oversee statements of work with relevant functions. Manage project budgets and forecasts, track invoices and proactively address variances against agreed scope, costs and timelines
• Coordinate CDMO and other external partner activities, follow up on deliverables and gather stakeholder input on vendor performance. Build effective relationships and resolve issues collaboratively
• Conduct line-of-business reviews of regulatory documentation supporting global submissions. Ensure technical compliance and timely delivery of source documentation in collaboration with subject matter experts and Regulatory Affairs
• Ensure adherence to Genmab’s quality system requirements. Understand the technical implications of supplier quality agreements, flag risks and coordinate follow-up with Quality and relevant functions

Project governance and ways of working

• Represent project management in internal and external forums. Communicate priorities, risks and recommendations, align stakeholders on decisions and ensure agreed actions are documented and followed through
• Use lessons learned to recommend and implement improvements to project management processes, systems and tools, strengthening consistency and operational effectiveness across the organization
• Train, mentor and guide colleagues in project management practices. Share experience and support effective project execution through informal leadership and constructive feedback

Requirements

• Master’s degree in science, engineering or a related technical discipline, or equivalent experience. An advanced degree or relevant certification is an advantage
• At least six years of experience in Tech Ops or a related field within a relevant industry, or an equivalent combination of education and experience
• Demonstrated success managing complex projects in a cross-functional environment, preferably within late-stage biologics development, with strong planning, budget and risk management skills
• Proven ability to influence and coordinate multicultural teams and internal and external stakeholders without direct authority
• Solid experience managing CDMOs and contract research organizations, with a strong understanding of intellectual property implications
• Sound knowledge of pharmaceutical regulations, GMP and regulatory documentation requirements, and their application to CMC project delivery.
• Experience implementing process or system improvements, with strong proficiency in project management systems, dashboards and reporting tools.
• Excellent written and verbal communication skills in English, with the ability to present complex topics and recommendations clearly

The role is based in Denmark. Travel is expected to be approximately 10–15 days per year.

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

The proposed gross annual/hourly base salary range for this position, in the primary location, based on a full time schedule is:

DKK644.640,00-966.960,00

The final salary offer will depend on several factors, including your skills, qualifications, and experience.

In addition to base salary, this position is eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to:

• Pension
• Health insurance and wellness benefits
• Paid time off
• Employee support programs

Further details on eligibility for compensation and benefits based on the role will be provided during the recruitment process.

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.

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