Site Research Assistant
hace 1 semana
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.
- 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.
- 2 years' relevant work experience in a clinical environment or medical setting. Experience as research 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
- Position On-site: Las Condes, Santiago
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