Clinical Research Associate (CRA) – Oncology Studies (6+ Months) - Sponsor dedicated - Türkiye

IQVIA · Istanbul, Turkey +1 more

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Role summary

IQVIA seeks an experienced Clinical Research Associate for oncology trials in Istanbul. The role involves monitoring clinical trial sites, managing regulatory compliance, coordinating subject recruitment, and maintaining study documentation according to GCP and ICH guidelines.

What they're looking for

Bachelor's degree in scientific or healthcare discipline, or equivalent education and experience
Minimum 6 months of on-site monitoring experience in oncology clinical studies
Previous CRA experience required
Solid understanding of GCP, ICH guidelines, and clinical research regulations
Proficiency in Microsoft Word, Excel, and PowerPoint
Strong written and verbal English communication skills
Excellent organizational, time management, and problem-solving abilities

What you'll be doing

Conduct site monitoring visits including selection, initiation, routine monitoring, and closeout activities
Ensure protocol compliance, patient safety, and regulatory adherence at trial sites
Track subject recruitment plans and support enrollment targets with sites
Deliver protocol training and maintain regular communication with investigative sites
Manage regulatory submissions, CRF completion, data queries, and Trial Master File documentation

Key requirements

Therapeutic area: Oncology

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Date posted16 days ago

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