Site Research Assistant - Durham, NC
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About The Position
IQVIA is seeking a Clinical Research Assistant to join our team, offering an immediate start for a period of 17 weeks, working 40 hours a week. This role is pivotal in supporting the site team and ensuring the smooth running of clinical trials. The Clinical Research Assistant will be responsible for a variety of tasks that include verifying and correcting research study information on source documents, resolving queries and variances, and providing feedback to the site data collector. The position requires accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures against the budget in the clinical trial management system (CTMS). Additionally, the role involves preparing and maintaining study files, timely submission of relevant regulatory and ethics documents, and scheduling visits with research subjects while generating appropriate reports and documentation. The Clinical Research Assistant will also engage in community outreach and recruitment efforts, which are essential for the success of clinical trials. This position requires strong organizational skills and attention to detail, as well as the ability to perform various administrative support functions such as reception duties, office organization, and supply management. The ideal candidate will have prior clinical research experience and a solid understanding of clinical trial processes, which will enable them to effectively support investigators and contribute to the overall success of the clinical research initiatives at IQVIA.
