Site Monitor Position

Há 5 dias

São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$45.000 - R$60.000

Clinical monitors are crucial professionals in the field of clinical research. They oversee the monitoring of clinical sites and ensure compliance with regulatory requirements.


Responsibilities
  • The role involves conducting routine monitoring visits at clinical sites to guarantee adherence to protocol guidelines and regulatory standards.
  • Maintaining accurate records of study site activities and data collected during monitoring visits is also a critical responsibility.
  • Identifying and addressing any deviations from protocol or regulatory requirements is essential for the smooth execution of studies.
  • Collaboration with site staff and vendors is necessary to resolve issues and ensure timely completion of studies.

Requirements
  • A university degree or certification in an allied health profession is typically required.
  • Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements are also essential.
  • Strong experience in clinical monitoring and site management is highly valued.
  • Excellent planning, organization, and problem-solving abilities are necessary for success in this role.

Working Conditions
  • Travel may be required for site visits and meetings.
  • The ability to work effectively in a matrix environment and with minimal supervision is also necessary.

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