Senior Clinical Research Associate

Há 5 dias


São Paulo, São Paulo, Brasil ICON Tempo inteiro
About the Role

As a Senior Clinical Research Associate at ICON, you will play a critical role in the success of our clinical trials. We are seeking an experienced and skilled professional to join our team and contribute to the delivery of high-quality clinical research services.

Key Responsibilities
  • Coordinate activities to set up and monitor clinical studies, ensuring adherence to applicable regulations and principles of ICH-GCP.
  • Submit protocol and consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals.
  • Balance sponsor-generated queries efficiently and ensure study cost-effectiveness.
  • Assist in training and mentoring less-experienced CRAs and/or lead CRAs working on international projects.
Requirements
  • 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 in English.
  • Ability to produce accurate work to tight deadlines within a pressurized environment.
  • Willingness to travel at least 60% of the time.
About ICON

ICON is a world-leading healthcare intelligence and clinical research organization. We are committed to fostering an inclusive environment that drives innovation and excellence. Our diverse teams enable us to become a better partner to our customers and help us fulfill our mission to advance and improve patients' lives.



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