Clinical Research Associate
IQVIA · Sofia, Bulgaria
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This position involves conducting site monitoring and management activities for clinical trials, including visit coordination, protocol training, recruitment oversight, and regulatory documentation. The role requires fluent Bulgarian and English, a scientific or healthcare background, at least one year of on-site monitoring experience, and strong knowledge of GCP and ICH guidelines.
What they're looking for
- Native Bulgarian language and English proficiency
- Bachelor's degree in scientific or healthcare discipline preferred
- Minimum 1 year on-site clinical trial monitoring experience
- Knowledge of GCP and ICH guidelines
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong written and verbal communication skills
- Organizational and problem-solving abilities
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities
- Develop and track subject recruitment plans with assigned sites
- Provide protocol training and maintain regular communication with study sites
- Evaluate study site quality and regulatory adherence, escalating compliance issues
- Manage study progress including enrollment tracking, data queries, and regulatory submissions
Privacy & handoff
This role links to IQVIA'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.