Clinical Research Associate

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

Experienced Clinical Research Associates

We are looking for Experienced Clinical Research Associates to join our team and support the successful execution of clinical trials by performing high‑quality monitoring and site management activities. In this role, you will ensure that study sites operate in compliance with protocols, GCP/ICH guidelines, regulatory requirements, and sponsor expectations while maintaining strong communication and collaboration with site staff and internal teams.

Responsibilities

• Conduct selection, initiation, monitoring, and close‑out visits according to GCP, ICH guidelines, and the contracted scope of work.
• Work with sites to develop and track subject recruitment plans aligned with project timelines.
• Provide protocol and study‑specific training to site personnel; maintain regular communication to support expectations and resolve issues.
• Assess site performance and ensure adherence to protocol, study procedures, and regulatory compliance; escal…
• Track study progress (regulatory submissions, approvals, enrollment, CRF completion, and data queries) and support start‑up activities when needed.
• Ensure essential documents are properly maintained in the TMF and verify ISF compliance with GCP and local regulatory standards.
• Document site management activities through timely monitoring visit reports, follow‑up letters, and required study documentation.
• Collaborate with cross‑functional study team members to support operational excellence.
• When applicable, support site‑level recruitment planning and site financial management.

Qualifications

• Bachelor’s degree in a scientific or healthcare discipline, or equivalent experience.
• Minimum of 1 year of on‑site monitoring experience.
• Good knowledge of GCP, ICH guidelines, and clinical research processes.
• Proficiency in Microsoft Word, Excel, PowerPoint, and digital tools.
• Strong written and verbal communication skills in English.
• Excellent organizational, time‑management, and problem‑solving abilities.
• Ability to build strong working relationships with sites, colleagues, and sponsors.

About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.