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Clinical Study Manager

1 mese fa

Milano, Lombardia, Italia Thermo Fisher Scientific A tempo pieno
Unlock Meaningful Work at Thermo Fisher Scientific

At Thermo Fisher Scientific, you'll embark on a journey that makes a lasting impact on a global scale. Our mission is to enable our customers to create a healthier, cleaner, and safer world. As a Clinical Study Manager, you'll be part of a team that accelerates research, solves complex scientific challenges, and drives technological innovation.

Key Responsibilities:
  • Provide quality oversight to Contract Research Organizations (CROs) and their deliverables related to study execution.
  • Lead and coordinate the execution of clinical trials from study start-up through database close and inspection readiness.
  • Develop and implement realistic recruitment targets and delivery milestones as the single point of accountability for detailed study start-up and monitoring plans.
  • Work closely with functional lines and directly with CRO line functions to resolve or triage site-level issues.
  • Drive decision-making and collaborate with Clinical Project Managers to provide input to operational strategy.
Requirements:
  • Minimum of 3 years of proven experience in study management or a related field.
  • Extensive global clinical trial/study management experience.
  • Working knowledge of Good Clinical Practices, monitoring, clinical, and regulatory operations.
What We Offer:

As a Clinical Study Manager at Thermo Fisher Scientific, you'll have the opportunity to work with a diverse team of 100,000+ colleagues who share a common set of values: Integrity, Intensity, Innovation, and Involvement. You'll be part of a company that values diverse experiences, backgrounds, and perspectives.

Join us in accelerating research, solving complex scientific challenges, and driving technological innovation. Apply your skills and expertise to make a meaningful impact on a global scale.