Junior Clinical Research Associate: Site Monitoring Training

IQVIA; Buenos Aires; On-site; ARS 54,524,000 - 72,699,000; Full time

Job summary

IQVIA in Buenos Aires, Argentina, offers a structured training program to gain knowledge and skills to independently conduct clinical monitoring visits in accordance with study protocol, SOPs, GCP, and regulatory requirements.

The role emphasizes training, supervision, site monitoring visits, regulatory tracking, TMF/ISF maintenance, and collaboration with study teams to support project delivery. Travel availability is required.

Qualifications

• Bachelor's Degree in scientific discipline or health care (Required).
• Monitoring course completed (Pref).
• Based in Buenos Aires (CABA / GBA).
• Availability to travel.
• Written and verbal communication skills including good command of English.
• Prior clinical experience preferred.
• Some organizations may require 2 years of clinical experience.

Responsibilities

• Perform site monitoring visits under supervision per protocol and SOPs.
• Complete appropriate training to perform job duties.
• Track regulatory submissions, recruitment, CRF completion, and data queries.
• Ensure TMF/ISF are maintained per GCP/ICH and local regulations.
• Create and maintain site management documentation and visit reports.
• Collaborate with study team for project execution support.
• Assist in startup phase and propose site recruitment ideas.

Skills

Good communication

Travel readiness

MS Word

MS Excel

PowerPoint

Time management

Problem solving

Team collaboration

GCP/ICH knowledge

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Laptops/iPhone usage

Job description

IQVIA in Buenos Aires, Argentina, offers a structured training program to gain knowledge and skills to independently conduct clinical monitoring visits in accordance with study protocol, SOPs, GCP, and regulatory requirements.

The role emphasizes training, supervision, site monitoring visits, regulatory tracking, TMF/ISF maintenance, and collaboration with study teams to support project delivery. Travel availability is required.