Experienced Clinical Research Associate Sponsor Dedicated - Cz Republic
IQVIA
Prague, Czech Republic
Site selection and initiation
Monitoring and close-out visits
Subject recruitment plan development
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, and supporting the development of a subject recruitment plan
Job Summary
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, and supporting the development of a subject recruitment plan.
You will evaluate the quality and integrity of site practices in accordance with regulatory requirements and manage progress by tracking regulatory submissions, recruitment, and data query resolutions.
IQVIA offers resources that promote your career growth, leaders that support flexible work schedules, and programs to help you build your therapeutic knowledge.
Matching Summary
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, and supporting the development of a subject recruitment plan.
Skills & Requirements
Must-have
site selection and initiation
monitoring and close-out visits
subject recruitment plan development
quality and integrity evaluation
progress tracking and management
collaboration with study sites and clients
Nice-to-have
organizational skills
time management skills
problem-solving skills
flexible work schedules
therapeutic knowledge building
Key Requirements
University degree in scientific discipline or health care
At least 1 year of experience as a Clinical Research Associate