Great opportunity if you want to join one of the greatest CROs and start your journey!
Job Overview
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.
- Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.
- Input visit data into clinical trial management system (CTM...
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IMS Saudi Arabia (SA01)
A leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.
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