CRA II

ICON plc • Blue Bell, SD

2d • Remote

About The Position

ICON is hiring a CRA II or Senior CRA for a U.S.-remote role. The position contributes to clinical trial monitoring, taking responsibility for assigned deliverables and working collaboratively. The CRA conducts site visits, supports protocol compliance, data integrity, and patient safety, and works with investigators and site staff to facilitate study conduct. The role also includes data review and query resolution, as well as contributing to study documentation, including protocols and clinical study reports. Travel is approximately 60% as required.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• At least 1 year 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, approximately 60%.
• 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.
• Perform data review 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