ICON plc

Clinical Research Associate – Ophthalmology

ICON plc

full-time

Posted on:

Location: 🇺🇸 United States

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Job Level

JuniorMid-Level

Tech Stack

Google Cloud Platform

About the role

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing 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.
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