Clinical Scientist – Manager/Senior Manager

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

• Support the Medical Director in the oversight of clinical studies including review and interpretation of clinical trial data • Take a lead role in writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies • Participate in the start-up of global clinical studies, working with Clinical Operations to ensure on schedule site activation and subject enrollment • Actively identify areas of emerging risk for the execution of clinical studies and proposing solutions to minimize and mitigate risk • Play a key role in the review of study data to ensure timely and high-quality data entry • Participate in investigator meetings, investigator engagement, including assisting in the preparation of Advisory Board meetings

🎯 Requirements

• BS or BSN is minimally required • An advanced degree in a scientific discipline (i.e. MS, PharmD, PhD, MD) is preferred • A minimum of 1 year of clinical development research in oncology or related clinical research experience within the industry (pharmaceutical, biotech, CRO) is required • Strong knowledge in clinical development in Oncology development is required • Significant experience with clinical evaluation projects including development of protocols, case report forms, informed consent and study initiation and monitoring • Significant experience with data integrity, exploration, analysis and presentation • High-performing and energetic individual who demonstrates outstanding scientific knowledge applicable to early disease clinical research and the highest personal and ethical standards • Self-organized, self-motivated, and able to work independently

🏖️ Benefits

• Professional development opportunities • Flexible working hours