Clinical Project 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 500 RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market.
 

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


Clinical Project Manager Vaccines /Oncology (f/m/d)
Kennziffer: 2102-2103

Your responsibilities:

  • Manage national and/or multinational clinical trials with innovative vaccines in the field of oncology/infectious diseases in close interaction with Contract Research Organizations (CROs)
  • Manage the budget, resources, and timelines associated with all study activities, including CRO/investigator agreements and other contractual agreements
  • Lead project teams through the start-up, study conduct, and report writing of clinical studies
  • Supervise the CRO and built up good working relationships with external stakeholders
  • Ensure the appropriate development of all documents internally and by the CROs, including study protocols, informed consent forms, case report forms and instructions, and other project-specific documents required for the conduct of assigned studies
  • Develop, write, and implement processes, systems, and Standard Operating Procedures (SOPs), to ensure quality and compliance with GCP and regulatory requirements
  • 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:

  • Masters degree in Life Sciences, otherwise equivalent education and work experience required
  • Extensive professional experience in clinical research at either a CRO, pharmaceutical or biotech company
  • Several years experience in clinical research ( at CRO and/or sponsor organisation) with some years experience in project management of clinical trials (preferably vaccines and/or oncology trials)
  • Understanding of the current national and international laws and guidelines regarding the conduct of clinical trials, specifically with ICH-GCP
  • Systematically perform activities in a timely and accurate manner
  • Service oriented approach; flexible and proactive attitude towards changing needs
  • Very good knowledge of MS Office Suite and MS Project
  • Fluency in English, German language skills are nice to have

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
Christina Glass
Friedrich-Miescher-Straße 15
72076 Tübingen