Clinical Trial Manager – Early Phase (f/m/d)

Jobbeschreibung

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

Clinical Trial Manager – Early Phase (f/m/d)


  • Clinical Trial Oversight and Management: Ensure compliance with GCP, SOPs, and regulations, manage recruitment across countries, and collaborate with LCRA to align the monitoring team with trial needs
  • Timeline and Resource Planning: Coordinate trial timelines with the CTL, plan resources like Veeva eTMF and co-monitoring, and ensure on-time trial execution and activity completion
  • CRO and Vendor Management: Oversee and evaluate CRO and service provider performance using KPIs, collaborate with the Vendor Management team, and assist in vendor selection and management
  • Document and Risk Management: Lead the creation and approval of essential trial documents, manage risk identification and mitigation, and track audit findings and CAPAs
  • Data Review and Reporting: Participate in ongoing and final data reviews, reporting issues or trends to the CTL
  • Team Leadership and Communication: Lead team meetings, provide training and mentorship to junior CRAs and new team members, and ensure effective communication between the sponsor, CRO, and other stakeholders

  • A university degree – preferably in Life Science, Chemistry, Biology or Pharmacy
  • Several years of proven professional experience in clinical research and the management of global clinical trials, with a strong emphasis on multinational oncology studies
  • Deep understanding and sound knowledge of ICH-GCP, FDA, EMA, and other relevant regulatory frameworks and guidelines
  • Solid background in oncology and a strong interest in new therapies
  • Proficiency with clinical trial management systems (CTMS), EDC, IRT systems, and eTMF
  • Strong communication and leadership skills, including experience managing CRO relationships
  • Excellent problem-solving abilities and a proactive approach to risk management
  • Ability to work independently within agreed goals and in a cross-functional team environment, providing constructive feedback
  • An independent, communicative, proactive, goal-oriented, and reliable work approach
  • Fluency in English
  • Willingness to travel internationally

  • 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
  • Comprehensive onboarding programme
  • Flexible working hours with home office options
  • Attractive special payments
  • Just a good salary? Not with us! We also offer you:
    • Employee participation programme
    • Job bike or subsidised job ticket
    • Above-average contribution to the company pension scheme
    • Individually tailored further training programme (including German and English courses)
    • Health promotion programmes (e.g. EGYM Wellpass, subsidy for local fitness studio, sponsorship of sporting events, various lifestyle coaching sessions)
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