Senior CRA II - Remote (US) Clinical Trials Expert

ICON Clinical Research; Center Square (PA); Remote; USD 75,000 - 120,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Job summary

ICON Clinical Research is seeking a CRA II or Senior CRA for a U.S. remote role. You will design and monitor clinical trials, interpret medical data, and contribute to advancing therapies.

Responsibilities include site qualification, initiation, monitoring, data review, and documentation support. The ideal candidate has a Bachelor’s in a scientific field and 1+ years in clinical research, with strong knowledge of ICH-GCP, and the ability to travel up to 60%.

Qualifications

• Experience in clinical trial monitoring and data review.
• Strong knowledge of ICH-GCP guidelines and trial processes.
• Excellent organizational and communication skills.
• Ability to travel up to ~60% as required.

Responsibilities

• Conduct site qualification, initiation, monitoring and close-out visits.
• Ensure protocol compliance, data integrity, and patient safety.
• Collaborate with investigators and site staff for smooth study conduct.
• Perform data review and resolve data queries.
• Contribute to study documentation such as protocols and CSRs.

Skills

Clinical trial monitoring

Data review

Site coordination

Regulatory compliance

Independent work

Education

Bachelor's degree in science/healthcare

Job description

ICON Clinical Research is seeking a CRA II or Senior CRA for a U.S. remote role. You will design and monitor clinical trials, interpret medical data, and contribute to advancing therapies.

Responsibilities include site qualification, initiation, monitoring, data review, and documentation support. The ideal candidate has a Bachelor’s in a scientific field and 1+ years in clinical research, with strong knowledge of ICH-GCP, and the ability to travel up to 60%.