Job Overview

Perform clinical research procedures and support study execution by collecting, recording, and interpreting data for participants enrolled or being screened for clinical studies. Ensure all activities follow study protocols, SOPs, and GCP guidelines. Contribute to daily workload planning and site operations.

Essential Functions

Support investigators in preparing for and conducting clinical studies

Review study materials, including protocols, CRFs, and EDC systems

Participate in study meetings and maintain study-related communication

Prepare and submit regulatory and ethics documentation (FDA and other authorities)

Recruit, screen, and orient study participants; maintain screening logs

Create and maintain source documents aligned with protocol requirements

Schedule and conduct study visits and perform protocol‑required procedures

Collect and manage study data ensuring accuracy, completeness, and compliance

Handle laboratory activities, including specimen preparation and logistics

Monitor participant safety and report adverse events appropriately

Respond to participant inquiries and resolve study‑related issues

Join daily huddles to align tasks and maintain operational standards

Assist with data quality checks and query resolution

Perform complex clinical procedures (ECG, sample collection, spirometry, vitals, dose verification, cannulation, telemetry monitoring)

Document and interpret study findings to support database development

Support investigators in meeting study timelines, budgets, and regulatory requirements

Train new site staff and maintain training documentation

Prepare for monitoring visits, audits, and regulatory inspections

Assist with staffing and scheduling planning for research activities

Qualifications

Bachelor’s degree required; or High School Diploma with equivalent experience

3 years of relevant clinical or medical experience (e.g., medical assistant, nurse assistant, lab technician)

Availability to work based in Rosario - Argentina Availability to work part-time (24 hours per week)Availability to work in a fixed term contract (6 months)

Working knowledge of clinical trials and Good Clinical Practice (GCP)

Strong understanding of protocols, SOPs, consent forms, and study schedules

Proficiency in clinical procedures (e.g., IV catheter insertion, spirometry)

Strong skills in MS Windows and Office (Access, Outlook, Word)

Excellent interpersonal communication abilities

High attention to detail

Ability to build and maintain effective working relationships with teams and clients

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.