Global Clinical Trials Coordinator

1 dia atrás


São Paulo, São Paulo, Brasil beBeeClinicalResearch Tempo inteiro R$40.000 - R$80.000
Role Summary">

The Clinical Research Associate (CRA) role plays a vital part in the clinical trials process, ensuring that studies are conducted efficiently and effectively.

Key Responsibilities:
  • Coordinate EC submissions and site activation activities, maintaining open lines of communication with stakeholders throughout South America.
  • Manage Informed Consent Forms (ICFs) to ensure compliance with regulatory requirements.
  • Update and maintain Clinical Trial Management systems (CTMS), streamlining data management processes.

This is a remote work opportunity, requiring strong interpersonal and communication skills. Fluency in English is essential for success in this role. The ideal candidate will have experience in clinical trials, preferably as a study nurse or site coordinator, and hold a degree in a health-related discipline.

A solid understanding of Good Clinical Practice (GCP) and relevant regulations is expected, along with knowledge of submission processes and Informed Consent Form customizations.



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