About this role
About the Role ICON is seeking a CRA II to design and analyze clinical trials, interpret complex medical data, and contribute to innovative treatments. The role focuses on clinical trial monitoring, ensuring data integrity and patient safety, and collaborating with investigators to facilitate study conduct. 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 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
- Competitive salary and range of benefits designed to support well-being and work-life balance.
- Various annual leave entitlements.
- Health insurance offerings.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme, LifeWorks (24/7 access to a network of professionals).
- Life assurance and flexible country-specific optional benefits (e.g., childcare vouchers, gym discounts, travel passes, health assessments).
- ICON is committed to inclusion, belonging, and equal opportunity for all candidates.