Unblinded CRA
ICON · Prague, Czechia
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Clinical Research Associate II for a Prague-based position in a sponsor-dedicated model. The role involves designing and analyzing clinical trials, monitoring sites, ensuring protocol compliance, and maintaining data integrity to support innovative treatment development.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of clinical research associate 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 fast-paced environment
- Willingness to travel approximately 60%
- Legal right to work in Czech Republic
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff to facilitate study conduct
- Perform data review and resolve queries to maintain high-quality clinical data
- Prepare and review study documentation including protocols and clinical study reports
Privacy & handoff
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