SiteResearchAssistant(CABA)

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 • Bachelor Degree in Health Sciences. Availability to work 24h per week for 6 months (Fixed Term) • Educational equivalent and 2 years’ relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience. • 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 • Excellent interpersonal skills • Ability to pay close attention to detail • Ability to establish and maintain effective working relationships with coworkers, managers and clients IQVIA is a leading global provider of clinical research services, commercial insights and hea