About this role
About the Role ICON is seeking a Clinical Research Associate (CRA) to join our team in Romania on a hybrid arrangement. You will contribute to clinical trial design and monitoring, interpreting complex medical data to advance innovative treatments, while delivering high-quality trial activities and collaborating with study teams. 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%). Nice to Have Compensation & Benefits
- Competitive salary and a range of benefits designed to support well-being and work-life balance.
- Various annual leave entitlements.
- Health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of professionals who support you and your family’s well-being.
- Life assurance.
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
- Visit our careers site to read more about the benefits ICON offers.