Discover a career with greater purpose

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.
• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.
• Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.

Qualifications
• High School Diploma or equivalent High School Diploma Req
• 1 year + of relevant work experience as research site assistant, study coordinator, or related position

• Intermediate level of English will be highly valued
• 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

• Part-time
• Fixed-term (6 months)
• Position on-site: Quilmes centro, Provincia de Buenos Aires.