по договоренности
Опыт от 3 до 6 лет

Job Responsibilities:

  • Coordinates/supports operational aspects for implementation of clinical trial activities from study start-up through database lock, ensuring quality and safety standards, regulations, timelines, budget commitments are met
  • Performs/coordinates protocol and site level feasibility activities, including evaluation of patient population and final sites selection (if applicable)
  • Provides input into and/or develops study related materials
  • Supports/coordinates negotiation of study budgets within FMV process, provides oversight of payments
  • Maintains effective and ongoing communication with CSM to manage or support day-to-day activities of the study, including monitoring reports review, problem solving, issue escalation, timely closure of non-productive sites, tracking of safety procedures
  • Supports management of country-level TMF and reviews for quality
  • Responsible for coordination and oversight of local affiliate study level audit/ inspection audit action plan activities
    • Work Environment:

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

      • University degree or equivalent, preferably in medical/ science-related field
      • Demonstrating knowledge and understanding of clinical trials
      • Monitoring experience is required
      • Previous experience managing projects is desirable
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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