CRA II

About this role

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Skills you'll use

What you'll do

• 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
• Bachelor's degree in a scientific or healthcare-related field.

Who can apply

• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Current or Prior experience in Therapeutic Areas like Oncology or Immunology or Gastroenterology or Pulmonology is a Must
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
• Rewards & Benefits
• ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Perks & benefits

About ICON plc

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