Clinical Research Associate – Oncology (6+ months)
iqvia · Istanbul
Job description
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.
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Published 2 gün önce
Expires 1 ay sonra
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iqvia
Istanbul