About this role
Job title: Clinical Research Associate II
About the Role Clinical Research Associate II at ICON is part of a world-leading healthcare intelligence and clinical research organization. ICON fosters an inclusive environment and drives innovation in clinical development. As a CRA II, you will design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments.
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 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 offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme with LifeWorks
- Life assurance and flexible country-specific optional benefits
- Additional perks such as childcare vouchers, bike purchase schemes, gym discounts, travel passes, and health assessments.