About this role
Job title: CRA II/Sr. CRA- CA/AZ
About the Role As a CRA II at ICON, you will design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments. This role focuses on site monitoring and ensuring the integrity and safety of the trial process.
What You'll Do
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure 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.
What We're Looking For
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 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 (approximately 60%).
Compensation & Benefits
- Salary range: $91,336.00-$114,170.00 USD per year.
- Benefits include bonuses, stock, health insurance options, retirement planning offerings, and access to LifeWorks global EAP.
- Global Employee Assistance Programme LifeWorks offers 24-hour access to a global network of professionals for you and your family.
- Life assurance and flexible country-specific optional benefits.
- ICON supports inclusion and belonging and provides accommodations on request.