Clinical Monitoring Specialist

1 semana atrás


São Paulo, São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

Job Summary

As a Clinical Monitoring Specialist at Thermo Fisher Scientific, you will play a critical role in ensuring the success of our clinical trials. Your primary responsibility will be to perform and coordinate all aspects of the clinical monitoring and site management process.

Key Responsibilities

  • Conduct remote or on-site visits to assess protocol and regulatory compliance
  • Manage required documentation and ensure accuracy and completeness
  • Develop and implement procedures and guidelines from different sponsors and/or monitoring environments
  • Act as a site processes specialist, ensuring that trial processes are outlined in the task matrix

Requirements

To be successful in this role, you will need to have a strong understanding of clinical trial regulations and guidelines, as well as excellent communication and organizational skills.

What We Offer

As a Clinical Monitoring Specialist at Thermo Fisher Scientific, you will have the opportunity to work on a variety of clinical trials and contribute to the development of new treatments and therapies.



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