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Urgent! Senior IRT Manager - Local Job Opening in Copenhagen

Senior IRT Manager



Job description

The Role

& Department


Genmab is seeking an experienced Senior IRT/System Manager to join our Global Clinical Drug Supply, Technical Operations team.

The position as IRT Manager is in Copenhagen.

The role requires onsite presence 3 days/week according company policy

With a strong pipeline and numerous ongoing clinical trials, you will play a key role in IRT Management—ensuring timely and high-quality clinical trial supplies for both early- and late-stage studies that support patients battling cancer and other serious diseases.

We are looking for proactive, solution-oriented professionals who thrive in dynamic environments, can balance priorities, and adapt quickly to change.

Our workplace is international, fast-paced, and collaborative—driven by a strong “one team” spirit both within and across departments.

Responsibilities

IRT Platform Management
• Define and maintain IRT standards, best practices, and training, in close alignment with governance for internal and external use
• Ensure compliance, qualification, validation, and ongoing oversight of Genmab’s IRT systems throughout their lifecycle
• Monitor vendor updates, identify process improvements, and contribute to streamlined timelines

IRT Portfolio & Project Management
• Oversee the full lifecycle of trial-specific IRT systems (setup, maintenance, decommissioning).
• Coordinate IRT implementation, protocol-driven requirements, UAT planning/execution, integrations, documentation, and training.
• Ensure adherence to IRT system standards and proactively manage risks.
• Oversee multiple projects, ensuring schedules and deliverables are met in collaboration with cross-functional stakeholders.
• Communicate project status effectively and participate in operational planning sessions.

IRT Vendor Management
• Act as Supplier Relationship Manager for IRT vendors.
• Support KPIs, metrics, and trend analysis to anticipate and mitigate risks.
• Provide oversight of vendor activities, ensuring quality and compliance.
• Collaborate with vendor project managers and participate in audits and inspection readiness.
• Facilitate problem resolution, root cause analysis, and corrective actions.

Continuous Improvement
• Identify opportunities to improve processes and lead assigned initiatives.
• Mentor and train IRT team members; support cross-functional training.
• Contribute to documentation development and maintenance (SOPs, work instructions, job aids).

Requirements
• Bachelor’s degree in a scientific or technical field; advanced degree/certification preferred.
• 6+ years’ experience in supply chain or related areas within pharma, biotech, or medical devices.
• Strong knowledge of regulatory standards (e.g., GMP, GCP, ICH).
• Hands-on experience with IRT systems.
• Proven ability to manage large, complex projects with multiple stakeholders.
• Experience working in cross-functional, multicultural teams.
 

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.


Required Skill Profession

Operations Specialties Managers



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