Site Research Assistant in Buenos Aires - IQVIA

IQVIA
IQVIA
Empresa verificada
Buenos Aires, Argentina

hace 1 semana

Sofía Rodríguez

Publicado por:

Sofía Rodríguez

beBee Recruiter
Descripción

Great opportunity if you want to join one of the greatest CROs and start your journey

Job Overview

Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.


Essential Functions

  • Provide clinical research support to investigators and site staff, including
  • Verify and/or correct research study information on source documents; research queries and variances; and provide
feedback to the site data collector.

  • Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,
accuracy, and completeness.

  • Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.
  • Collect and submit regulatory/ethics documentation pertaining to the research study.
  • Maintain the FDA 1572 form for assigned research studies.
  • Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.

Qualifications

  • Availability to work on site (La Plata, Buenos Aires, Argentina).
  • Bachelor's degree (ideal).
  • Study coordinator experience or similar (with some knowledge in clinical trials).
  • Intermediate/Advanced level of English.
LI-NRJ #LI-Onsite
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