
Biotechnology • Pharmaceuticals
Tubulis GmbH is a biotechnology company specializing in the design and development of next-generation antibody–drug conjugates (ADCs) for cancer treatment. The company leverages proprietary platform technologies to generate uniquely matched ADCs with improved biophysical properties, durable on-tumor delivery, and strong preclinical anti-tumor activity. Its lead clinical programs, TUB-040 (anti-NaPi2b) and TUB-030 (anti-5T4), target high-need solid tumor indications, and Tubulis advances both its proprietary pipeline and partnered programs with the aim of expanding the therapeutic potential of ADCs for patients and collaborators.
October 13

Biotechnology • Pharmaceuticals
Tubulis GmbH is a biotechnology company specializing in the design and development of next-generation antibody–drug conjugates (ADCs) for cancer treatment. The company leverages proprietary platform technologies to generate uniquely matched ADCs with improved biophysical properties, durable on-tumor delivery, and strong preclinical anti-tumor activity. Its lead clinical programs, TUB-040 (anti-NaPi2b) and TUB-030 (anti-5T4), target high-need solid tumor indications, and Tubulis advances both its proprietary pipeline and partnered programs with the aim of expanding the therapeutic potential of ADCs for patients and collaborators.
• Lead outsourced packaging, labeling, and distribution of CTM to support global clinical trials. • Ensure timely, compliant delivery of investigational products in partnership with CMC, Clinical Operations, QA, and Regulatory Affairs. • Translate study requirements into supply plans, manage inventory across depots, and maintain IRT systems. • Develop budgets, forecasts, and risk assessments, providing updates to SVP CMC. • Procure comparator/commercial products as needed and oversee global logistics. • Ensure vendor compliance and collaborate with CMC/QC on expiry management. • Serve as the primary point of contact for all CTM supply chain activities and provide strategic input as programs move into late-stage development.
• Bachelor’s or Master’s degree in Supply Chain, Drug Development, or related field with 12+ years’ experience in Clinical Supply Management. • Experience managing global clinical supply, including early- and late-phase trials and working with CMOs. • Strong knowledge of clinical protocols, IRT systems, and regulatory requirements (GMP, ICH, 21 CFR, Annex 13). • Hands-on expertise in forecasting, supply-demand planning, and inventory management. • Excellent project management, organizational, and communication skills. • Ability to thrive in a matrix environment, handle shifting priorities, and collaborate with cross-functional teams. • Willingness to travel (up to 20%) and work flexible hours as needed.
• Impact that matters : Contribute to breakthrough therapies. • Global mindset : Work in an international, diverse team. • Grow & thrive : Develop your career in a supportive, fast-moving environment. • Innovation every day : Push boundaries with cutting-edge science.
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