Clinical Study Manager

22 ore fa


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

We are seeking a highly skilled Clinical Study Manager to join our team at Thermo Fisher Scientific. As a key member of our clinical operations team, you will be responsible for leading and coordinating the execution of clinical trials from start-up to close-out.

Key Responsibilities
  • Provide quality oversight to Contract Research Organizations (CROs) and ensure timely delivery of quality study data.
  • Lead and coordinate the execution of clinical trials, including study start-up, monitoring, and close-out.
  • Develop and implement realistic study start-up and monitoring plans, as well as study delivery plans.
  • Work closely with functional lines and directly with CRO line functions to resolve or triage site-level issues.
  • Drive decision-making and provide input to operational strategy.
Requirements
  • Master's or Ph.D. degree in a relevant field, with a minimum of 3 years of proven experience, or a Bachelor's or Nurse degree with a 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.
What We Offer

At Thermo Fisher Scientific, we offer a dynamic and supportive work environment, with opportunities for professional growth and development. We are committed to enabling our customers to make the world healthier, cleaner, and safer.

As a Clinical Study Manager, you will have the opportunity to work on complex projects, collaborate with cross-functional teams, and contribute to the development of innovative solutions. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.



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