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Clinical Project Manager

2 mesi fa

Milano, Lombardia, Italia Thermo Fisher Scientific A tempo pieno
About the Role

As a Clinical Project Manager at Thermo Fisher Scientific, you will play a key role in planning and executing clinical trials from start to finish. Your primary responsibility will be to provide quality oversight to Contract Research Organizations (CROs) and ensure timely delivery of quality study data.

Key Responsibilities
  • Provides quality oversight to CROs and ensures timely delivery of quality study data
  • Leads and coordinates the execution of clinical trials from start-up through database close and inspection readiness
  • Works with functional lines and directly with CRO line functions to resolve or triage site-level issues
  • Drives decision-making and works closely with the Clinical Project Manager to provide input to operational strategy
  • May be required to act as 'lead' study manager and coordinate activities of other Study Managers assigned
Requirements
  • MS/PhD – minimum of 3 years of proven experience
  • BS/Nurse – minimum of 5 years of proven experience
  • Extensive global clinical trial/study management experience
  • Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations
  • Expertise in one or various tech areas, specializing in driving innovation and efficiency through technology
  • Demonstrated study management/leadership experience with oversight of CROs
  • Demonstrated experience in managing Per Subject Costs, vendor & ancillary, and monitoring costs projections & spend
What We Offer
  • A dynamic and collaborative work environment
  • Opportunities for professional growth and development
  • A competitive salary and benefits package
  • The chance to work on complex and challenging projects