"Clinical Study Manager"

2 settimane fa


Milano, Lombardia, Italia Thermo Fisher Scientific A tempo pieno

About the Role:

As a Clinical Study Manager at Thermo Fisher Scientific, you will be responsible for the execution of clinical trials from start-up to database close. Your expertise in study management and leadership will enable you to oversee the delivery of quality study data and drive innovation through technology.

Key Responsibilities:

  • Provide quality oversight to Contract Research Organizations (CROs) and their deliverables.
  • Lead and coordinate the execution of clinical trials, ensuring timely delivery of quality data.
  • Develop and implement study start-up and monitoring plans, setting realistic recruitment targets and delivery milestones.
  • Work with vendors to accomplish tasks, interpreting study-level data and identifying risks.
  • Drive decision-making and collaborate with Clinical Project Managers to provide input to operational strategy.

Requirements:

  • MS/PhD or BS/Nurse with minimum 3/5 years of proven experience in global clinical trial/study management.
  • Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations.
  • Expertise in one or various tech areas, specialising in driving innovation and efficiency through technology.

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