Team Lead Java Development; m​/w​/d

ITM is a privately owned biotechnology and radiopharmaceutical group of companies dedicated to the development, production and global supply of targeted diagnostic and therapeutic radiopharmaceuticals and radioisotopes for use in cancer treatment. We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone metastases. Our main objectives are to significantly improve treatment outcomes and quality of life for cancer patients through a new generation of Targeted Radionuclide Therapies in Precision Oncology.

The headquarters are located in the heart of the research center of the Technical University of Munich (TUM).

We would like to fill the following permanent vacancy in a hybrid working model in Garching as soon as possible

• Serve as Regulatory Affairs expert for early-stage development projects within the radiopharmaceutical pipeline, with a primary focus on upcoming IND/CTA submissions, reporting directly to the Head of Clinical Regulatory Affairs
• Act as the primary regulatory contact with key Health Authorities (FDA, EMA), holding operational accountability for regulatory interactions and submissions in close collaboration with subject matter experts and the Global Project Team (GPT)
• Lead the preparation and conduct of scientific Health Authority meetings (Pre-IND, Type A–D, EMA Scientific Advice, Protocol Assistance) and oversee timely preparation, submission, and approval of original and amendment filings (INDs, CTAs) in the US, EU, and other regions
• Develop and implement global regulatory strategies for assigned product candidates in alignment with the clinical development plan and overall program objectives
• Plan, organize, and manage regulatory activities in line with global development plans and regulatory milestones, including identification of risks and implementation of mitigation strategies for complex radiopharmaceutical products
• Coordinate timely, high‑quality responses to Health Authority requests and ensure the use of appropriate regulatory pathways to optimize submission strategies
• Provide regulatory input, review, and approval of key clinical and non‑clinical documents, including study protocols, Investigator’s Brochure (IB), Clinical Study Reports (CSR), and non‑clinical reports
• Author and review high‑quality, product‑specific regulatory documents (e.g., meeting requests, briefing books, iPSPs, orphan annual reports) in close collaboration with cross‑functional experts, ensuring compliance with regional regulatory requirements
• Provide clear, proactive regulatory guidance to clinical trial teams using an “out‑of‑the‑box” mindset, maintain strong cross‑functional stakeholder collaboration, stay current with evolving regulatory guidelines, and support non‑program‑specific initiatives (e.g., business development, departmental projects, training)

• Successfully completed scientific studies (Bachelor’s or Master’s degree) in pharmacy, chemistry, biochemistry, biotechnology, or a related field; a post‑graduate degree is an advantage
• A minimum of 7–10 years of experience in regulatory roles within the pharmaceutical or biotechnology industry or at a regulatory authority
• Profound knowledge and hands‑on experience with regulatory requirements for pharmaceutical development, with a strong focus on IND and CTA regulations applicable to clinical development
• Proven ability to understand, interpret, and strategically integrate oncology drug development regulations and guidelines into comprehensive development plans; experience with radiopharmaceuticals is a strong asset
• Experience in direct interactions with regulatory authorities, in particular with the FDA and EMA
• Excellent written and spoken English skills; fluency in German is a plus

• Exciting challenges in an up‑and‑coming and fast‑growing company with a high degree of creative freedom
• An open working atmosphere in an international corporate culture with short communication channels
• Flexible working hours with home office options
• Attractive special…