About this role
Job title: Study Start-Up CRA
About the Role ICON is seeking a Study Start-Up CRA to design and analyze clinical trials, interpreting complex medical data, and support innovative treatments within a global pharma environment. You will focus on study start-up activities for cardiology trials and collaborate across sites and sponsors.
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 approximately 60%
Compensation & Benefits
- Competitive salary and benefits package
- Various annual leave entitlements
- Health insurance options and retirement planning offerings
- Global Employee Assistance Programme with 24/7 support
- Life assurance and flexible country-specific optional benefits (e.g., childcare vouchers, travel discounts, gym memberships)
- ICON is committed to inclusion and a discrimination-free workplace.