Clinical Research Coordinator

hace 5 días


Santiago, Metropolitana, Chile IQVIA Argentina A tiempo completo

Job Overview

IQVIA is seeking a highly organized and detail-oriented Clinical Research Coordinator to support clinical trials in Las Condes, Santiago. As a key member of our team, you will provide administrative assistance to investigators and site staff, ensuring the smooth execution of research studies.

Responsibilities:

  • Verify and correct research study information on source documents; respond to research queries and variances;
  • Input research study data into the trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness;
  • Prepare and maintain research study files, compiling, collating, and submitting 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;
  • Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits;
  • Input visit data into the clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.

Qualifications

  • Bachelor's degree or equivalent required;
  • At least 2 years of relevant work experience in a clinical environment or medical setting;
  • Intermediate level of English proficiency highly valued;
  • Familiarity with clinical trials and departmental operating procedures preferred;
  • Basic knowledge of medical terminology;
  • Proficiency in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.


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