Site Research Assistant

hace 1 semana


Santiago, Metropolitana, Chile IQVIA Argentina A tiempo completo

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

  1. Provide clinical research support to investigators and site staff, including
  2. Verify and/or correct research study information on source documents; research queries and variances; and provide feedback to the site data collector.
  3. Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness.
  4. Prepare and maintain research study files. 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.
  8. Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.

Qualifications

  1. High School Diploma or equivalent.
  2. 2 years' relevant work experience in a clinical environment or medical setting. Experience as research assistant, study coordinator, or related position.
  3. Intermediate level of English will be 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.
  • Part-time
  • Position On-site: Las Condes, Santiago
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