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Clinical Research Associate

2 meses atrás

São Paulo, São Paulo, Brasil ICON Tempo inteiro
{"title": "Senior Clinical Research Associate", "content": "Role Summary

As a Senior Clinical Research Associate at ICON, you will play a key role in the success of our clinical trials. Your primary responsibility will be to coordinate and monitor clinical studies, ensuring adherence to regulatory requirements and ICH-GCP guidelines.

Key Responsibilities
  • Coordinate and monitor clinical studies, including site initiation, monitoring, and close-out.
  • Ensure compliance with regulatory requirements and ICH-GCP guidelines.
  • Collaborate with cross-functional teams to identify and mitigate risks.
  • Develop and maintain study documentation, including study protocols and informed consent forms.
  • Provide training and support to less experienced CRAs.
Requirements
  • Minimum 24 months of monitoring experience in phase I-III trials as a CRA.
  • Knowledge of ICH-GCP guidelines and expertise to review and evaluate medical data.
  • Excellent written and verbal communication skills in English.
  • Ability to work independently and as part of a team.
  • Willingness to travel at least 60% of the time.
What We Offer

At ICON, we offer a competitive salary package, health-related benefits, and a comprehensive retirement plan. We are an equal opportunity employer and are committed to providing a workplace free of discrimination and harassment.

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