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Site Research Assistant, Part-time
hace 3 semanas
This is an on-site position in Quilmes centro, Provincia de Buenos Aires, part-time and fixed-term _
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
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.
- Review Charts from Site Database; Update Study Portals
- Patient Management such as education, visit scheduling and reminders, prescreen referrals
- Community outreach
**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
- ** Part-time (24 hours weekly)**
- ** Fixed-term (6 months)**
- ** Position on-site (presencial)**:_Quilmes centro, Provincia de Buenos Aires_
