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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 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

• Availability to work on site (Santa Fe capital, Argentina).

• Availability to work part-time (20 hours a week)

• Availability to work in a fixed-term contract (6 months)

• Bachelor's degree (ideal).
• Study coordinator experience or similar (with some knowledge in clinical trials).
• Intermediate/Advanced level of English.

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