Clinical Trials Coordinator

hace 5 días


Santiago, Metropolitana, Chile ICON Strategic Solutions A tiempo completo

About the Job:

We are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and SOPs.

Responsibilities:

  • Conducting onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes
  • Verifying the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance with applicable regulations
  • Writing and submitting reports of investigational site findings and updates applicable tracking systems
  • Escalating observed deficiencies, issues, and corrective and preventative action plans as appropriate
  • Participating in audit preparation and follow-up activities as needed

Requirements:

  • Bachelor's degree in a health, life sciences, or other relevant field of study
  • Previous experience supporting clinical trials including 1 year of on-site monitoring experience
  • Previous experience in oncology is a plus
  • Travel is required
  • All employees must read, write, and speak fluent English and host country language

About ICON Strategic Solutions:

We are a leading provider of clinical research solutions, committed to improving patient outcomes through innovative and collaborative approaches.



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