About this role
About the Role ICON is seeking a Clinical Research Associate II (CRA II) based in Spain to support design, analysis and monitoring of clinical trials. You will contribute to the advancement of innovative treatments by conducting monitoring visits, ensuring data integrity and patient safety, and collaborating with investigators to drive study success.
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 3 years of experience as a Clinical Research Associate.
- Oncology solid tumors 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.
- Willingness to travel as required (approximately 60%).
Compensation & Benefits
- Competitive salary and a range of additional 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.
- Global Employee Assistance Programme with 24-hour access to a global network of professionals.
- Life assurance and flexible country-specific optional benefits.
- ICON is committed to inclusion, equal opportunity, and a workplace free of discrimination.