100%, as soon as possible, limited for 18 months

Your responsibilities

  • Proactive support of all aspects of one or more phase 1-4 clinical studies (for Covid-19 vaccine or for Lyme vaccine development)
  • Support in the implementation of clinical studies from start-up to study completion
  • Contribution to the development of study relevant documents in the project development cycle
  • Monitoring and execution of all study activities in compliance with ICH-GCP and FDA/EMA/MHRA requirements
  • Cross-functional collaboration with internal and external stakeholders (e.g. CROs)
  • Support in budget planning and financial tracking

Your qualifications

  • Academic education, Master or PhD degree (Life Science)
  • At least 1 year of relevant experience as a CRA in the pharma/life science industry
  • Project management experience is an advantage
  • Ideally experience in the field of vaccine development as well as supervision of CROs and CRAs
  • Team oriented, stress resistant personality
  • Strong communication and organizational skills
  • Ability to prioritize and maintain oversight
  • Very good command of English (spoken and written)

Our offer

  • Open, appreciative company culture with innovative spirit and attractive assignments
  • International surrounding with flat hierarchies
  • Good team spirit in a strong and highly motivated team
  • Wide range of benefits like flexitime, performance-related bonus, lunch vouchers, child care center (“Kindergarten”), company events

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 50.000,-  gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.

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