Clinical Research Associate with experience - Sponsor dedicated - Serbia
IQVIA · Belgrade, Serbia
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate position focused on sponsor-dedicated monitoring and site management for clinical trials. The role involves conducting site visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across assigned studies in Serbia.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline preferred
- 1+ years of CRA and on-site monitoring experience
- Fluent written and verbal communication in English and Serbian
- Strong organizational and problem-solving abilities
- Valid driver's license and ability to travel to sites
- IT proficiency and effective time management skills
What you'll be doing
- Conduct site selection, initiation, monitoring, and close-out visits
- Work with sites on subject recruitment planning and tracking aligned with project objectives
- Deliver protocol training and maintain ongoing communication with study sites
- Evaluate study site practices for protocol adherence and regulatory compliance
- Track study progress including recruitment, CRF completion, 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.