Clinical Research Associate

IQVIA; Fatih; On-site; TRY 420,000 - 580,000; Full time

Job summary

A leading clinical research organization in Turkey is seeking Experienced Clinical Research Associates to ensure the execution of clinical trials through high-quality monitoring and site management. Responsibilities include conducting visits, assessing site performance, providing training to site staff, and maintaining compliance with protocols and regulations. Ideal candidates will have a scientific degree and at least one year of on-site monitoring experience. Strong English communication skills are essential.

Qualifications

• Minimum of 1 year of on-site monitoring experience.
• Good knowledge of GCP, ICH guidelines, and clinical research processes.
• Fluent in English, both written and verbal.
• 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.

Responsibilities

• Conduct selection, initiation, monitoring, and close‑out visits.
• Work with sites to track subject recruitment plans.
• Assess site performance and ensure compliance with regulations.
• Assess site performance and ensure adherence to protocol, study procedures, and regulatory compliance; engage quality escalation when appropriate.
• 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.

Skills

GCP knowledge

Strong communication skills

Organizational skills

Time-management skills

Problem-solving abilities

Education

Bachelor's degree in a scientific or healthcare discipline

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Digital tools

Job description

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; engage quality escalation when appropriate.
• 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.

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.