CRA II

ICON plc • Blue Bell, SD

3d

About The Position

At ICON Strategic Solutions, the CRA II works in a sponsor-dedicated model supported by ICON’s global expertise. The role contributes to clinical trial monitoring and the development of treatments that benefit patients worldwide. This is a six-month assignment.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• At least 2 years of experience as a Clinical Research Associate.
• 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.
• Willingness to travel as required.
• Comfortable with a six-month assignment.
• Must have the legal right to work in the country where the role is based.

Responsibilities

• 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.
• Review data and resolve queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Benefits

• Competitive base salary and performance-related incentives.
• Medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level