Tubulis GmbH
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.
Associate Medical Director – Medical Director
October 13
Tubulis GmbH
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.
📋 Description
• Provide clinical leadership and strategic medical input for clinical deliverables in the assigned project • Lead clinical sections of trial and program level regulatory documents • Act as clinical lead within the clinical trial team • Execute clinical development strategy in line with regulations • Support overall safety of the molecule and contribute to safety reporting • Develop clinical standards for new disease areas • Prepare reports on clinical trials such as abstracts and manuscripts • Support preclinical functions in developing biomarker strategies • Identify and mitigate technical, clinical, and financial risks to the program • Maintain communication with non-clinical development teams for product goals • Develop and maintain scientific and clinical knowledge in respective areas.
🎯 Requirements
• MD, MD/Ph.D. in life sciences and Oncology Fellowship training required • 3+ years of experience in a pharmaceutical or biotechnology environment • Experience in biologics/ADC clinical development • Strong track record in clinical teams for global Phase I-IV trials • Experience writing protocol amendments, informed consents, and other clinical study documents • Knowledge of oncology and ability to interpret safety and efficacy data from clinical trials • Solid understanding of GCP, clinical trial design, and regulatory processes • Ability to establish effective scientific partnerships with key partners • Experience with management of KOLs and CROs, and in conducting clinical ad boards • Experience with generation of scientific publications. • Expertise in programming in R (preferred qualification).
🏖️ Benefits
• Health insurance • Flexible working hours • Professional development opportunities
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