ICON plc

Clinical Research Associate

ICON plc

full-time

Posted on:

Origin:  • 🇺🇸 United States • Kansas, Missouri

Visit company website
✨ AI Apply
Manual Apply

Job Level

JuniorMid-Level

Tech Stack

Google Cloud Platform

About the role

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborate with investigators and site staff to facilitate smooth study conduct
  • Perform data review and resolution of queries to maintain high-quality clinical data
  • Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

  • Bachelor's degree in a scientific or healthcare-related field (highly preferred)
  • Minimum of 2 years of experience as a Clinical Research Associate (on site monitoring experience required)
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment