Clinical Research Associate

hace 6 días


Santiago, Metropolitana, Chile ICON Strategic Solutions A tiempo completo

At ICON Strategic Solutions, we are committed to providing high-quality services in clinical research. As a Clinical Research Associate (CRA), you will play a crucial role in ensuring the integrity of our studies and protecting the rights of study participants.

Key Responsibilities:
  • Conduct on-site monitoring activities to verify compliance with ICH-GCP guidelines, applicable regulations, SOPs, and study protocols.
  • Review informed consent procedures and ensure that they are conducted in accordance with applicable regulations.
  • Verify the accuracy and completeness of clinical data and ensure that it is collected and reported in compliance with approved protocols, GCP, and applicable regulations.
  • Prepare and submit reports of investigational site findings and update tracking systems accordingly.
  • Evaluate and escalate observed deficiencies, issues, and corrective actions as necessary.
Requirements:
  • Bachelor's degree in a health-related field, such as life sciences or a related discipline.
  • At least one year of experience supporting clinical trials, including on-site monitoring.
  • Prior experience in oncology is an asset.
  • Travel is required for this position.
  • Fluency in English and the host country language is essential.


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