Clinical Research Associate – Oncology Studies (6+ Months)

About the role

IQVIA Turkey is seeking an experienced Clinical Research Associate (CRA) dedicated to oncology studies. The role involves on‑site monitoring and site management to ensure trials are executed in line with protocol, regulations and sponsor expectations.

Key responsibilities

• Perform monitoring visits including site selection, initiation, routine monitoring and close‑out in accordance with GCP and ICH guidelines.
• Drive and track subject recruitment plans to meet project timelines.
• Deliver protocol‑specific training to investigative sites and maintain regular communication.
• Evaluate site compliance with protocol, patient safety and regulatory requirements, escalating issues as needed.
• Track regulatory submissions, enrollment status, CRF completion and data query resolution.
• Ensure essential documents are complete in the Trial Master File and Investigator Site File.
• Prepare accurate monitoring visit reports, follow‑up letters and action plans.
• Collaborate with cross‑functional study team members to support overall project delivery.

Required profile

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

Required skills

• Proficiency in Microsoft Word
• Proficiency in Microsoft Excel
• Proficiency in Microsoft PowerPoint