Clinical Trial Manager (f/m/d)

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 470 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 Manager (f/m/d)
Job-ID: 2102-2003

Your responsibilities:

  • Assisting in identification, selection and hiring of appropriate CROs and third-party vendors and support third-party vendor training on protocols and practices
  • Support of identifying, selecting, and monitoring performance of investigational sites for clinical trials including negotiation and management of investigational site payments
  • Overseeing performance of CROs, third-party vendors, and field CRAs including co-monitoring to ensure compliance with study protocol; identifying areas of concern and escalating to CPM
  • Preparing and supporting investigator meetings
  • Reviewing key study quality metrics (e.g. eligibility, primary endpoint data etc.) and determining appropriate action in conjunction with study team
  • Tracking and reporting on study progress including site activation, subject/patient enrollment, monitoring visits, and relevant documents
  • Writing or contributing to preparation of clinical protocols, amendments, informed consent forms, study guides, case report forms, and any other clinical research-related documents

Your qualifications:

  • Master´s degree in Life Sciences, otherwise equivalent education and work experience required
  • 5 years experience in clinical research (at CRO and/or sponsor organization) with at least 2 years experience in on-site monitoring of interventional clinical trials (preferably oncology and/or vaccine trials)
  • At least 1 year of trial management experience
  • Solid knowledge of clinical study processes, Good Clinical Practice (GCP) and other regulatory guidelines
  • Basic knowledge of project management and clinical research budgets, including processing and tracking of site and vendor payments, would be an advantage
  • The ability to support several projects simultaneously, a flexible working style and attention to detail are essential
  • Strong knowledge of MS Office and MS Project
  • Fluency in English, German is a plus
  • Willingness to travel up to 15%

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
Mr. Gregor Zimmermann
Friedrich-Miescher-Straße 15
72076 Tübingen