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Clinical Trial Manager

Tel Aviv


  • Involve in all stages of the company’s clinical trials, including setting up potential sites, initiating, monitoring and closing the trial. Responsibilities includes, but not limited to:
    • Responsibility for the preparation of study-related documents including regulatory processes
    • Maintain GCP Compliance in the company’s clinical activities via periodical co-monitoring, audits issues and inspections activities
    • Assess quality of work of sub-contractors including monitoring visits, co-monitoring or oversight visits with CROs, protocol deviation management, and on-regular-basis communications with the study centers personnel 
  • Account for all clinical documents including protocols (content and accuracy)
  • Interact and manage the interpersonal and professional relationships with the medical teams and with other disciplines inside and outside the company
  • Contribute to improvement of processes, systems, and tools as well as infrastructure of the company’s clinical operations
  • Contribute to the development and review of clinical SOPs
  • The role may include managing clinical procedures in cath-lab environment
  • Ability to travel – 20% of the time

Minimum Qualifications:

  • B.S. degree in Life Sciences or equivalent
  • 3+ years of experience in as a clinical trials manager (preferred in cardiology)
  • Understanding of and compliance to applicable regulations and guidelines
  • Strong understanding of GCP

Preferred Qualifications:

  • Ability to work independently and prioritize projects with little supervision
  • Excellent written and verbal communication skills, including proficiency in medical terminology from several disciplines
  • Strong multitasking ability with impeccable attention to details
  • Excellent analytical, organizational, and problem-solving skills
  • Relationship management skills
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