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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
- 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
- Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,
- 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.
- Prepare and maintain study supplies.
- 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.
- Review Charts from Site Database; Update Study Portals
- Patient Management such as education, visit scheduling and reminders, prescreen referrals
- Community outreach
- Upkeep regulatory binder
- High School Diploma
- 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 (16 hours weekly)
- Fixed-term (6 months)
- Position on-site (presencial): Ciudad Autónoma de Buenos Aires
Key Skills
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