(senior) Clinical Research Associate - Sponsor Dedicated - Türkiye
IQVIA UK
Istanbul, Türkiye
Site selection, initiation, monitoring, close-out
Subject recruitment plan development
Gcp and ich guidelines adherence
You will gain direct experience with one of IQVIA's customers while enjoying the stability and resources of a leading, global contract research organization
Job Summary
You will gain direct experience with one of IQVIA's customers while enjoying the stability and resources of a leading, global contract research organization.
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits, supporting subject recruitment, and evaluating site practices.
IQVIA offers resources that promote career growth, supportive leaders, programs to build therapeutic knowledge, and a better work-life balance in a stable, international company.
Matching Summary
You will gain direct experience with one of IQVIA's customers while enjoying the stability and resources of a leading, global contract research organization.
Skills & Requirements
Must-have
site selection, initiation, monitoring, close-out
subject recruitment plan development
GCP and ICH guidelines adherence
regulatory submissions tracking
case report form completion
data query resolution
Nice-to-have
career growth resources
flexible work schedules
therapeutic knowledge building
optimal work-life balance
excellent working environment
Key Requirements
University degree in scientific discipline or health care
At least 2 years on-site monitoring experience
Good knowledge of clinical research regulatory requirements