CRA2, IQVIA Biotech Argentina

ARG IQVIA RDS Argentina SRL; Buenos Aires; On-site; ARS 1,200,000 - 1,800,000; Full time

Job summary

IQVIA Biotech Argentina is seeking a dedicated Clinical Research Associate (CRA) to join our team. The CRA will monitor clinical sites to ensure protocol adherence, regulatory compliance, and data integrity, contributing to high-quality trial execution on-site.

The role requires at least 1 year of on-site monitoring experience, strong knowledge of GCP/ICH guidelines, and willingness to travel as needed. Collaboration with cross-functional teams is essential for project success.

Qualifications

• Must have a bachelor’s degree in life sciences or health-related field.
• At least 1 year of on-site monitoring experience.
• Strong understanding of GCP, ICH guidelines, and regulatory requirements.
• Willingness to travel as required by the project.

Responsibilities

• Conduct site visits—selection, initiation, monitoring, and close-out per scope, GCP, and ICH.
• Collaborate with site staff to implement recruitment strategies aligned with timelines.
• Deliver protocol and study-specific trainings to site personnel.
• Assess site performance and escalate quality concerns to ensure data integrity.
• Monitor regulatory submissions, subject enrollment, CRF completion, and data queries.
• Ensure TMF and ISF are complete and compliant with regulatory standards.
• Document site activities, visit outcomes, and follow-up actions in reports.
• Work with cross-functional teams to support study execution and project goals.
• Support site-level recruitment planning and budget tracking when required.

Skills

On-site monitoring

Education

Bachelor’s degree in life sciences or health-related field

Job description

IQVIA Biotech Argentina is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine: IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.

Key Responsibilities

• Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
• Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
• Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
• Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
• Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
• Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
• Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
• Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
• Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.

Qualifications

• Bachelor’s degree in life sciences or health-related field (or equivalent experience).
• Requires at least 1 year of on-site monitoring experience.
• Strong understanding of GCP, ICH guidelines, and regulatory requirements.
• Ability to travel as required by the project.

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.