Associate Director, Supply Chain

The Associate Director, Team Lead, Global Clinical Drug Supply (GCDS) is responsible for leading the strategic, operational, and organizational aspects of the team across an assigned portfolio. This role ensures the development, integration, and execution of robust forecasting, demand planning, and supply strategies to effectively support clinical trials, while maintaining compliance with regulatory requirements and company quality standards. As a team leader and member of the extended leadership team, this position plays a critical role in shaping the organization, driving internal and external cross-functional alignment, and enabling efficient, standardized, and scalable ways of working within the functional area. Work arrangement for Princeton, NJ and Copenhagen, DK: 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. Global Clinical Drug Supply - Planning 34; Contribute to the definition, implementation, and execution of standards for drug supply planning, ensuring alignment with departmental strategy, portfolio needs, and regulatory requirements 34; Establish and continuously refine forecasting methodologies, assumptions, and demand planning approaches for IMP/AxMP across projects and trials 34; Lead the development, implementation, and ongoing optimization of SOPs, ensuring alignment with evolving regulatory requirements and enabling scalable and efficient ways of working 34; Drive and encourage strategic planning and continuous improvement initiatives across the GCDS organization to enhance efficiency, integration, and execution 34; Ensure strong cross-functional integration and alignment across GCDS (Planning, Manufacturing, and Systems) to support seamless supply execution 34; Act as a senior strategic partner to internal stakeholders (Clinical Operations, CMC, Medical, Portfolio Management) and external partners (CROs and other collaborators) People Leadership & Team Development 34; Lead, develop, and inspire the team, fostering a high-performing, collaborative, and accountable culture 34; Provide leadership, coaching, and mentoring to team members, ensuring continuous development of performance and capabilities 34; Collaborate with the Functional Lead and Co-Team Leads to shape and evolve the team structure, enabling efficient, scalable, and future-ready ways of working 34; Drive standardization, integration, and optimization of processes across the functional area 34; Contribute to the alignment of team goals, roles, and strategic initiatives with company objectives and portfolio priorities 34; Act as the escalation point for the drug supply planning team and cross-functional challenges, ensuring timely and effective resolution Project & Trial Supply Management 34; Lead strategic and operational drug supply planning for clinical programs and trials 34; Act as project manager for key compounds and programs, ensuring standardization, consistency, and alignment across trials 34; Support the development, integration, and maintenance of high-level supply strategies, forecasts, and demand plans across the trial lifecycle 34; Guide and support the team in maintaining continuous oversight of supply to prevent stock-outs and ensure timely delivery of clinical materials 34; Oversee and support the monitoring and optimization of inventory levels to minimize waste and cost Requirements 34; Bachelors degree or equivalent, preferably within life sciences, supply chain, procurement, pharmaceutical sciences, engineering, business, or a related field. 34; 12+ years of experience from a regulated biotech, pharma clinical supply, supply chain, or similar environment. 34; Proven people leadership experience, with the ability to coach, develop, and motivate others. 34; Demonstrated ability to balance team leadership with hands-on contribution as a subject matter expert. 34; Extensive knowledge and understanding of GMP, GDP, GCP, and documentation standards in a regulated environment. 34; Proven ability to drive cross-functional projects and collaborate effectively in global, virtual, and matrixed teams. 34; Strong ability to prioritize, create structure, and drive decisions in a fast-paced environment with tight timelines and competing priorities. 34; Curious, self-driven, and confident in challenging assumptions, escalating risks, and speaking up when something does not add up. 34; Strong communication skills in English, both oral and written. For US based candidates, the proposed salary band for this position is as follows: $153,440.00---$230,160.00 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, youre 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: 34; 401(k) Plan: 100% match on the first 6% of contributions 34; Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance 34; Voluntary Plans: Critical illness, accident, and hospital indemnity insurance 34; Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave 34; Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support 34; Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses Further details on eligibility for compensation and benefits based on role will be provided during the recruitment process