Clinical Research Associate

IQVIA · Istanbul, Turkey

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks experienced Clinical Research Associates to support clinical trial execution in Istanbul. The role involves site monitoring, protocol compliance oversight, and coordination with research sites to ensure adherence to GCP/ICH guidelines and regulatory requirements.

What they're looking for

Bachelor's degree in scientific or healthcare field, or equivalent experience
Minimum 1 year of on-site clinical monitoring experience
Knowledge of GCP, ICH guidelines, and clinical research processes
Proficiency in Microsoft Word, Excel, PowerPoint, and digital tools
Strong written and verbal English communication skills
Excellent organizational, time-management, and problem-solving abilities
Ability to establish collaborative relationships with sites and teams

What you'll be doing

Conduct site selection, initiation, monitoring, and close-out visits per GCP standards
Develop and track subject recruitment plans aligned with project timelines
Provide protocol training to site personnel and maintain regular communication
Monitor site performance for protocol adherence and regulatory compliance
Document and report monitoring activities, follow-ups, and study progress

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Date posted16 days ago

Last source check1 day ago

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