Clinical Research Coordinator in Córdoba
hace 4 semanas
Unlock Your Potential in Clinical Research
Clinical Research Coordinators play a vital role in supporting investigators and site staff in the conduct of clinical trials. As a Clinical Research Coordinator in Córdoba, you will be responsible for providing administrative support to ensure the smooth execution of clinical trials.
Key Responsibilities
- Verify and correct research study information on source documents, research queries, and variances, and provide feedback to the site data collector.
- Input research study data into the 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 the clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.
Requirements
- Availability to work on site in Córdoba, Argentina.
- Availability to work part-time.
- 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.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://www.iqvia.com/"
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