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Clinical Research Coordinator in Bs As

hace 1 mes

Buenos Aires, Argentina IQVIA A tiempo completo

**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.
- 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 (Bs As, Quilmes).
- Availability to work part-time (20 hours weekly)
- 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.