Clinical Research Associate II - Remote

Overview

The Clinical Research Associate II at ICON plays a pivotal role in designing and analyzing clinical trials, ensuring protocol compliance, and contributing to innovative treatments.

In Short

• 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.
• Must have a Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes and regulations.
• Strong organizational and communication skills.
• Ability to travel at least 60% of the time.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum 2 years of experience in clinical research.
• Knowledge of ICH-GCP guidelines.
• Strong attention to detail.
• Ability to work independently and collaboratively.
• Valid driver’s license.

Benefits

• Competitive salary and benefits package.
• Various annual leave entitlements.
• Health insurance offerings.
• Retirement planning offerings.
• Global Employee Assistance Programme.
• Flexible optional benefits.