Associate Medical Director – Medical Director

October 13

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Tubulis GmbH

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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

📋 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