About this role
Job title: Senior CRA / CRA II - Home-Based (United States)
About the Role ICON is seeking a Senior Clinical Research Associate or CRA II to join ICON's diverse and dynamic team in a home-based role in the United States. As a CRA at ICON, you will play a pivotal role in designing and monitoring clinical trials, interpreting complex medical data, and advancing innovative therapies.
What You'll Do
- 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, including protocols and clinical study reports.
What We're Looking For
- Bachelor's degree in a scientific or health-related field or equivalent experience in clinical research (e.g., study coordinator or nursing).
- Minimum of 1 year independent monitoring for CRA II; minimum of 3 years independent monitoring for Senior CRA.
- 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.
- Ability to travel at least 60% of the time (international and domestic) with a valid driver’s license.
Compensation & Benefits ICON offers a competitive salary and a range of benefits designed to support well-being and work-life balance, including various annual leave entitlements, health insurance options, retirement planning, LifeWorks global EAP, life assurance, and flexible country-specific benefits. ICON is committed to inclusion and equal opportunity for all applicants.