по договоренности
Опыт от 3 до 6 лет

Job Responsibilities:

  • Responsibility for execution and oversight of clinical trial submissions and approvals for assigned protocols
  • Development of local documentation
  • Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Agreements (Sites, Investigators)
  • Responsibility for clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management
  • Ability to proactively develop risk management and mitigation plans and resolve all start-up related issues
    • Work Environment:

    • Competitive compensation, salary rate is under discussion
    • Medical insurance
    • Car allowance
    • Office-based work
      • Requirements:

      • Bachelor's Degree (or comparable) in Finance/ Administration/ Life Science or equivalent Health Care related experience
      • A minimum of 3 years of Start-up / Regulatory experience
      • Fluent in local languages of the countries under responsibilities and upper-intermediate English
      • Extensive knowledge of local regulatory environment and submission and approval processes
      • Strong communication, problem solving and leadership skills
      • Background in business finance will be a plus as well as strong knowledge and aptitude in accounting and financial procedures
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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