Clinical Research Associate – Oncology (6+ months)

About the role

IQVIA Turkey seeks an experienced Clinical Research Associate to support oncology studies on a sponsor‑dedicated basis. The CRA will ensure trials are conducted in line with protocols, regulations and sponsor expectations.

Key responsibilities

• Perform site monitoring visits—including selection, initiation, routine monitoring and close‑out—following GCP and ICH guidelines.
• Drive subject recruitment plans, track enrollment, CRF completion and data query resolution.
• Maintain essential documents in the Trial Master File and ensure Investigator Site Files comply with local regulations.
• Prepare monitoring reports, follow‑up letters and action plans, and collaborate with cross‑functional study teams.

Required profile

• Bachelor’s degree in a scientific or healthcare discipline (or equivalent experience).
• Minimum 6 months of on‑site monitoring experience in oncology clinical studies.
• Strong understanding of GCP, ICH guidelines and clinical research regulations.
• Excellent written and verbal English communication skills.

Required skills

• Proficiency with Microsoft Word.
• Proficiency with Microsoft Excel.
• Proficiency with Microsoft PowerPoint.