About this role
About the Role ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. This role is based in Vancouver, Canada with opportunities for travel. What You'll Do
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring 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 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience.
- 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 - fly and drive) and should possess a valid driver’s license. Compensation & Benefits
- Competitive salary and benefits focused on well-being and work-life balance, including various annual leave entitlements, a range of health insurance offerings, competitive retirement planning, Global Employee Assistance Programme LifeWorks, life assurance, flexible country-specific optional benefits, and more.
- ICON is committed to inclusion & belonging and equal opportunity employment.