CRA 2 (Clinical Research)

Location: Buenos Aires, Argentina

Company

IQVIA Biotech is a full-service contract research organization serving biotech sponsors with therapeutically aligned clinical research solutions.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits according to the contracted scope, GCP, and ICH guidelines.
• Collaborate with site staff on subject recruitment strategies, enrollment targets, protocol training, and issue resolution.
• Assess site performance, protocol adherence, regulatory submissions, CRF completion, and data-query resolution.
• Collect and maintain essential documents in the Trial Master File and Investigator Site File.
• Document site activities, visit outcomes, follow-up actions, and correspondence.
• Support recruitment planning, invoice collection, budget tracking, and cross-functional study execution as required.

Requirements

• Bachelor’s degree in life sciences or a health-related field, or equivalent experience.
• At least 1 year of on-site monitoring experience is required.
• Experience in oncology, cardiovascular, or internal medicine therapeutics.
• Strong understanding of GCP, ICH guidelines, and regulatory requirements.
• Ability to travel as required by the project.

Culture & Benefits

• Work on clinical research programs supporting the development of innovative medical treatments.
• Collaborate with biotech sponsors, clinical sites, and cross-functional project teams.
• Contribute to clinical data quality, regulatory compliance, and improved patient outcomes.