Site Research Assistant

hace 2 semanas

Buenos Aires, Argentina IQVIA A tiempo completo

Job Overview (Part-Time, Fixed-Term Role)


Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures
at a field-based clinical site 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 fieldbase in Buenos Aires city
  • Availability to work parttime
  • Availability to work in fixed term contract
  • High School Diploma or equivalent required.
  • Educational equivalent and 2 years' relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training, and experience required.
  • Basic knowledge of clinical trials.
  • Indepth knowledge of departmental, protocol, and studyspecific operating procedures, consent forms, and study schedules.
  • Basic knowledge of medical terminology.
  • Excellent interpersonal skills.

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