About ITM

We would like to fill the following vacancy in a hybrid or remote working model as soon as possible:

Your Role:

• Nuclear Medicine Expertise: develop expertise in targeted radiotherapy, including diagnostic and therapeutic agents (theranostics), within the medical team
• Clinical Development Support: key role in designing and executing early and late Clinical Development projects, collaborating closely with preClinical Development
• Protocol Development and Safety Oversight: Support the development of clinical study protocols, ensuring compliance with international regulations, with a focus on imaging and dosimetry and collaborate with the Drug Safety Team to monitor compound safety in Clinical Development
• Technology Integration: work with the Nuclear Medicine Lead and dosimetry team to develop and utilize in-house Hermes image viewer and dosimetry platform for Clinical projects
• Scientific Support and External Engagement: Provide scientific support across the development portfolio, contributing to due diligence, early development, and commercialization and represent Nuclear Medicine externally with experts, regulatory authorities, and advisory boards
• Clinical Development Activities: Support Clinical Medical Lead(s) in study strategy, design, data analysis, interpretation, and report generation
• Regulatory Contribution and Study Oversight: Contribute to regulatory submissions, including IND/CTA, NDA/BLA/MAA, DSUR, and INDSRs and manages ongoing studies, ensuring effective communication with sites, stakeholders, and regulatory bodies.

What we are looking for:

• Physician (f/m/d) specialized in Nuclear Medicine with theranostic experience
• Ability to manipulate and interpret Nuclear Medicine images. Background with segmentation tools and dosimetry expertise is encouraged
• First professional work experience in a drug/biologic developing company, ideally in oncology indication or as clinical investigator in industry sponsored trials
• Ability to work in a hierarchically flat, matrix environment
• Strong working knowledge of the clinical drug development process, clinical trial design, data management (including CDISC standards) and biostatistics
• Ability to understand, integrate, analyse and interpret clinical data
• Good management, interpersonal, communication, negotiation and problem-solving skills
• Fluency in English

What we offer:

• A modern workplace and exciting opportunities in an evolving and fast growing company
• Challenging and varied projects in interdisciplinary, multicultural and highly professional teams
• A collegial corporate culture and short communication channels
• Flexible working hours with an attractive salary package and diverse corporate benefits

At ITM, we work together towards one common goal - the benefit of our patients. This is what drives us, every day. This is what we are passionate about. For this we create opportunities that are as unique as our team. We encourage diversity and inclusion – the input of our multi-cultural employees makes us who we are.
Only together we can contribute to significantly improving the outcome and quality of life of cancer patients worldwide and to giving better answers than "maybe”.
Does this sound like you? Are you interested in shaping the future of ITM and joining one of our highly committed teams in an innovative work environment?
Then send us your detailed CV including earliest start date and salary expectations. Applications are accepted either in English language.

Human Resources