Experienced Clinical Research Associate - Sponsor Dedicated - Türkiye
IQVIA
Türkiye
Site selection and monitoring
Regulatory compliance and guidelines
Subject recruitment planning
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, supporting the development of a subject recruitment plan, and evaluating the quality and integrity of site practices
Job Summary
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, supporting the development of a subject recruitment plan, and evaluating the quality and integrity of site practices.
You will manage progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions, while collaborating with experts at study sites and with client representatives.
IQVIA offers resources that promote your career growth, leaders that support flexible work schedules, programs to help you build your therapeutic knowledge, and an excellent working environment in a stable, international, reputable company.
Matching Summary
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, supporting the development of a subject recruitment plan, and evaluating the quality and integrity of site practices.
Skills & Requirements
Must-have
Site selection and monitoring
Regulatory compliance and guidelines
Subject recruitment planning
Data query resolution
Excellent command of Turkish and English
Nice-to-have
Career growth opportunities
Flexible work schedules
Therapeutic knowledge building
International reputable company
Key Requirements
University degree in scientific discipline or health care
At least 6 months on-site monitoring experience
Experience in Pharma Industry and/or Clinical Trials