(senior) Clinical Research Associate - Sponsor Dedicated - Türkiye
IQVIA
Istanbul, Türkiye
Site selection and monitoring
Gcp and ich guidelines
Tracking regulatory submissions
You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers
Job Summary
You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
Your responsibilities will include performing site selection, initiation, monitoring and close-out visits.
What you can expect: Resources that promote your career growth, Leaders that support flexible work schedules, Programs to help you build your therapeutic knowledge, Better Work-Life balance, optimal DOS, Excellent working environment in a stabile, international, reputable company.
Matching Summary
You’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
Skills & Requirements
Must-have
site selection and monitoring
GCP and ICH guidelines
tracking regulatory submissions
Excellent command of Turkish and English
Nice-to-have
flexible work schedules
building therapeutic knowledge
optimal DOS
effective working relationships
Key Requirements
University degree in scientific discipline
At least 2 years on-site monitoring experience
Good knowledge of clinical research regulatory requirements