(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

IQVIA · Istanbul, Turkey +1 more

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks a senior clinical research associate in Istanbul to serve as a sponsor-dedicated monitor. The role involves site management, regulatory compliance oversight, and cross-functional collaboration across clinical trials.

What they're looking for

University degree in scientific or healthcare discipline
Minimum 2 years on-site clinical trial monitoring experience
Knowledge of GCP, ICH guidelines, and clinical research regulations
Proficient in MS Office and computer systems
Fluent in Turkish and English
Valid Class B driver's license
Strong organizational and problem-solving abilities

What you'll be doing

Conduct site selection, initiation, monitoring, and closeout visits
Develop and support subject recruitment planning strategies
Verify site compliance with GCP and ICH regulatory standards
Track trial progress including submissions, enrollment, CRF completion, and data queries
Liaise with site investigators and sponsor representatives

CompensationSign-on bonus up to 210,000 TRY for candidates starting before September 2026

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Date posted17 days ago

Last source check1 day ago

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