Senior Clinical Research Associate
ICON · Sofia, Bulgaria
Clinical OperationsFull-timeCompany career page
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Role summary
ICON seeks a Senior Clinical Research Associate to design and analyze clinical trials while monitoring study sites and ensuring protocol compliance. The role involves managing trial initiation through close-out, collaborating with investigators, and maintaining data integrity across clinical research programs.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum 5 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulations
- Strong organizational and communication skills with meticulous attention to detail
- Ability to work independently and collaboratively in fast-paced environments
- Willingness to travel approximately 60% as required
What you'll be doing
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial processes
- Collaborate with investigators and site staff to facilitate effective 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
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.