Clinical Research Associate

IQVIA Argentina; Fatih; On-site; TRY 180,000 - 280,000; Full time

Job summary

IQVIA is seeking an Experienced Clinical Research Associate to support the execution of clinical trials through monitoring and site management, ensuring sites comply with protocols, GCP/ICH, and regulatory requirements. You will collaborate with site staff and internal teams, manage visits, training, and recruitment plans, and help maintain TMF and ISF documentation.

This role requires a scientific or healthcare degree, 1 year on-site monitoring, and strong English communication; experience with

Qualifications

• Bachelor's degree in a scientific or healthcare field or equivalent.
• Minimum 1 year of on-site monitoring experience.
• Solid knowledge of GCP, ICH guidelines, and clinical research processes.
• Proficient with Word, Excel, PowerPoint and digital tools.
• Strong written and spoken English communications.

Responsibilities

• Conduct selection, initiation, monitoring, and close-out visits according to GCP/ICH.
• Develop and track subject recruitment plans aligned with timelines.
• Provide protocol and site training; maintain regular communications.
• Assess site performance and ensure adherence to protocol and regulation.
• Track study progress and support start-up activities when needed.
• Maintain TMF and verify ISF compliance with standards.
• Document site management activities via monitoring reports and letters.
• Collaborate with cross-functional study team members for operational excellence.
• When applicable, support site recruitment planning and site financial management.

Skills

GCP/ICH knowledge

Site monitoring

Clinical operations

English communication

Microsoft Office

Education

Bachelor's degree in science/healthcare

Tools

Microsoft Word

Microsoft Excel

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; escalate quality issues 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.