Site Research Assistant at Pereira, Colombia

at  IQVIA

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.

• 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 providefeedback 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.