Clinical Research Associate 1 or 2 (m/w/d), Single Sponsor
IQVIA · Hesse, Germany
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks Clinical Research Associates (CRA I or II) for remote positions across Germany within their single sponsor department. The role involves site management, regulatory compliance oversight, and study coordination for clinical trials, with opportunities for professional development and specialization across therapeutic areas.
What they're looking for
- University degree in life science or scientific discipline, or healthcare apprenticeship
- Minimum 12 months on-site clinical monitoring experience
- Knowledge of GCP and ICH regulatory guidelines
- German language fluency at C1 level; strong English proficiency
- Excellent written and verbal communication with attention to detail
- Valid class B driver's license
- Willingness to travel 40-60% of working time
What you'll be doing
- Conduct site selection, initiation, monitoring, and close-out visits
- Support subject recruitment planning and track study progress metrics
- Ensure site compliance with GCP, ICH, and applicable regulatory requirements
- Manage regulatory submissions, CRF completion, and data query resolution
- Collaborate with study sites and client representatives on trial execution
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.