Clinical Trial Supply Manager (f/m/d)

Design. Progress. Together.


CureVac Manufacturing GmbH, a wholly owned subsidiary of CureVac SE, is a biopharmaceutical company producing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on innovative cancer immunotherapies, prophylactic vaccines and molecular therapies. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market.


To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a


Clinical Trial Supply Manager (f/m/d)


Your tasks: 


  • Oversight of the life cycle of the Investigational Medicinal Product (IMP) - from receipt to IMP destruction - including label design, packaging and distribution 
  • Planning, coordination and monitoring of clinical trial material such as IMP and Ancillaries, related activities to ensure efficient and compliant supply including documentation according to processes and regulatory requirements 
  • Support the selection, release, training and surveillance of qualified distribution sites in close collaboration with the project and line functions 
  • Development, supervision and optimization of required manuals and provision of input to other related documents, as required 
  • Coordination and management of deviations, which are related to storage and/or transport of clinical trial material 
  • Support the coordination, ensure timely completion, documentation and communication of deviations from product requirements, processes or documentation, in alignment with relevant internal and external stakeholders 
  • Contribution to continuous improvement of processes under your responsibility 


Your profile: 


  • Scientific degree, e.g., in chemistry, biology, pharmacy, medicine or equivalent 
  • Extensive experience in clinical research and management of clinical trials 
  • Proven experience in at least one of the following areas, preferably in combinations: Life cycle management of investigational products as well as in GMP or GCP, project and process management 
  • Experience in guiding, or training colleagues and setting goals is an advantage 
  • Solid understanding of processes combining big picture risk management with attention to detail 
  • Highly motivated, open-minded team player with a proven ability to take initiative, prioritize and meet timelines in a very dynamic environment. Problem solving attitude. 
  • High communicative skills 
  • Fluency in English, German is a plus 


We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding.
With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us.

Design your future with us – become part of the RNA people!   

We look forward to receiving your application via our CareerPortal.


CureVac Manufacturing GmbH


Human Resources
Gregor Zimmermann 
Friedrich-Miescher-Straße 15
72076 Tübingen