Clinical Research Coordinator
hace 2 semanas
Clinical research support specialists play a vital role in the success of clinical trials. As a Site Research Assistant at IQVIA Argentina, you will provide administrative support to investigators and site staff.
Key Responsibilities- Verify and/or correct research study information on source documents; research queries and variances;
- 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;
- High School Diploma or equivalent High School Diploma required;
- Educational equivalent and 2 years' relevant work experience in a clinical environment or medical setting, preferably as a research assistant, study coordinator, or related position;
- Intermediate level of English highly valued;
- BASIC knowledge of clinical trials;
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules;
- BASIC knowledge of medical terminology;
- BASIC skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word;
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