Clinical Research Associate – Monitoring & Site Leadership

IQVIA; Fatih; On-site; TRY 230,000 - 320,000; Full time

Job summary

IQVIA is seeking Experienced Clinical Research Associates to join our team to ensure clinical trial sites operate in accordance with protocols, GCP/ICH guidelines, and regulatory requirements. You will monitor sites, manage relationships with site staff and sponsors, and support study activities across multiple projects.

The role requires at least 1 year of on-site monitoring experience, strong communication skills in English, and a solid understanding of clinical research processes.

Qualifications

• Bachelor's degree in a scientific or healthcare field.
• Minimum 1 year of on-site monitoring experience.
• Strong knowledge of GCP/ICH guidelines and clinical research processes.

Responsibilities

• Conduct selection, initiation, monitoring, and close‑out visits per GCP/ICH guidelines.
• Develop and track subject recruitment plans aligned with project timelines.
• Provide protocol training to site personnel and maintain regular communication.

Skills

GCP/ICH knowledge

On-site monitoring

Site management

Clinical research processes

English communication

Education

Bachelor's degree in life sciences

Tools

Microsoft Word

Excel

PowerPoint

Job description

IQVIA is seeking Experienced Clinical Research Associates to join our team to ensure clinical trial sites operate in accordance with protocols, GCP/ICH guidelines, and regulatory requirements. You will monitor sites, manage relationships with site staff and sponsors, and support study activities across multiple projects.

The role requires at least 1 year of on-site monitoring experience, strong communication skills in English, and a solid understanding of clinical research processes.