Clinical Research Coordinator

hace 2 semanas


Santiago, Metropolitana, Chile IQVIA Argentina A tiempo completo
Job Overview

Clinical research support specialists play a vital role in the success of clinical trials. As a Site Research Assistant at IQVIA Argentina, you will provide administrative support to investigators and site staff.

Key Responsibilities
  1. Verify and/or correct research study information on source documents; research queries and variances;
  2. Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness;
  3. Prepare and maintain research study files;
  4. Compile, collate and submit study information within established deadlines;
  5. Collect and submit regulatory/ethics documentation pertaining to the research study;
  6. Maintain the FDA 1572 form for assigned research studies;
  7. Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits;
Requirements
  1. High School Diploma or equivalent High School Diploma required;
  2. Educational equivalent and 2 years' relevant work experience in a clinical environment or medical setting, preferably as a research assistant, study coordinator, or related position;
  3. Intermediate level of English highly valued;
  4. BASIC knowledge of clinical trials;
  5. In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules;
  6. BASIC knowledge of medical terminology;
  7. BASIC skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word;


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