Clinical Trial Supply Manager (f/m/d)

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Design. Progress. Together.

CureVac AG is a biopharmaceutical company researching and developing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on innovative cancer immunotherapies, prophylactic vaccines and molecular therapies. Currently, about 600 RNA people are striving to achieve our main goal: To bring the first mRNA-based drug worldwide to the market.

To strengthen our team in Frankfurt am Main, we are currently looking to recruit a

Clinical Trial Supply Manager (f/m/d)
Job-ID: 2101-2102

Your responsibilities:

  • Develops demand forecasts and clinical trial supply (CTS) strategies and plans, including timelines and budgets
  • Manage CTS demand per trial, advising team of potential shortages and making recommendations for resupply activities based on usage trends
  • Manages / co-ordinates external clinical trial supply vendors and logistic vendors
  • Manage the preparation, handling, distribution, filing and archiving of Clinical Trial Services (CTS) documentation
  • Accurately maintain various CTS tracking spreadsheets (general and study specific), by ensuring  appropriate documentation of CTS activities is provided for the Trial Master File
  • Manage activities related to clinical supply, incl. labeling, packaging, distribution activities, reconciliation and destruction of clinical supply materials (IMP and ancillaries)
  • Communicate with internal and external parties as needed
  • Design label text meeting product requirements and ensure compliance with international regulations
  • Coach new CTS team members. Lead training efforts on CTS processes to facilitate improved cross-functional relationships
  • Identifying and supporting strategies for continuous improvement and departmental and/or inter-departmental projects

Your qualifications:

  • Comprehensive experience in the CRO, pharmaceutical or biotech industry
  • Results-oriented approach, flexible and proactive attitude towards changing needs; willingness to work on different projects simultaneously
  • Works independently, systematically perform activities in a timely and accurate manner
  • Knowledge of the current national and international laws and guidelines regarding the conduct of clinical trials, specifically with ICH-GCP. Knowledge of GMP/GCP/GLP regulations
  • Experience and interest in working in a dynamic team environment with multiple activities
  • Very good knowledge of MS Office
  • Fluency in English; German is a plus

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 AG

Human Resources
Ms Christina Glass
Friedrich-Miescher-Straße 15
72076 Tübingen