
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.
51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
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.
51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
• 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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