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Clinical Project Manager m/f/d




  • Forschung
  • Projektmanagement

Gewünschte Studienfächer

  • Biotechnologie


  • Bachelor
  • Master/Diplom


  • Hechingen

As a steadily growing international manufacturer of high quality vascular implants, we help surgeons save lives. For this reason, we are looking for committed employees (m/f/d) who will work enthusiastically and ambitiously to find the best possible solution for the patient and the user.

What you bring to the position:

  • Degree in natural sciences, medicine or medical technology
  • At least 1-2 years of experience as a Clinical Project Manager (m/f/d) in the planning and implementation of international clinical studies with medical devices in Europe and Asia-Pacific
  • Experience with regulatory audits (FDA experience desirable)
  • Experience in negotiating study contracts
  • Very good knowledge of the relevant national and international regulations
  • Excellent organisational and administrative skills
  • Motivating, respectful communication internally and with business partners and investigators
  • High level of commitment to reach the expected objectives

What you will be doing:

  • Planning and conducting international clinical studies, ensuring study teams deliver against time and quality
  • Monitoring CROs and regularly drafting reports on the status of studies
  • Regulatory approvals and approvals by ethics committees in Europe and Asia
  • Preparing study contracts
  • Organising and conducting investigator meetings
  • Safety notices and coordination of the clinical evaluation committee (CEC)

What you can expect:

  • An exciting and steadily growing product portfolio for vascular therapy
  • Varied tasks within a dynamic team
  • Freedom for ideas and independent work
  • Intensive training in areas of responsibility

Apply today:
Ina Müller, jobs.europe@cryolife.com, T: 07471 922 441
JOTEC GmbH, Lotzenäcker 23, 72379 Hechingen

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