Research Assistant

hace 2 semanas


Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo

Job Overview

This role involves providing administrative support for clinical trials, working closely with investigators and site staff to ensure accurate and timely data collection and management.

Key Responsibilities:

  1. Provide research study support to investigators and site staff, including verifying and correcting study information and inputting data into the EDC system
  2. Prepare and maintain research study files, compiling and submitting study information within established deadlines
  3. Collect and submit regulatory/ethics documentation pertaining to the research study
  4. Maintain the FDA 1572 form for assigned research studies
  5. Schedule subject visits and generate reports and documents for research subjects prior to visits

Qualifications

  • High School Diploma or equivalent
  • 1 year + of relevant work experience as research site assistant, study coordinator, or related position
  • Intermediate level of English
  • Basic knowledge of clinical trials
  • In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word


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