по договоренности
Опыт от 1 до 3 лет

Job Responsibilities:

  • Responsible for site feasibility, site selection and qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance to Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs)
  • Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel
  • Develop, review and edit clinical trial related documentation including but not limited to; Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists
  • Perform pre-study initiation, interim monitoring and close out visits as required
    • Work Environment:

    • Competitive compensation and benefit program
    • Salary rate is under discussion
    • Medical insurance
    • Car allowance
      • Requirements:

      • Medical Doctor (MD) degree or Pharmacist would be your advantage
      • A minimum 2-year experience as a Clinical Research Associate
      • Travel required
      • Fluent in local languages of the countries under responsibilities and upper-intermediate English
      • Thorough understanding of standard operating procedures, clinical research principles and process
      • Energetic, active personality and ability to also work independently and to effectively prioritise tasks
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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