Provide support for clinical research to investigators and site staff, including:
Verify and correct research study information on source documents, research queries, and variances; provide feedback to the site data collector.
Input research study data into trial Electronic Data Capture (EDC) system, ensuring 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 related to the research study.
Maintain the FDA form for assigned research studies.
Schedule subject visits and generate appropriate reports and documents for research subjects before visits.
Input visit data into the clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.
Qualifications
High School Diploma or equivalent High School Diploma Required
Educational equivalent and 2 years of relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training, and experience Required
Basic understanding of clinical trials
In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
Basic familiarity with medical terminology
Basic proficiency in using MS Windows and Office applications like Access, Outlook, Excel, and Word
Strong interpersonal skills
Ability to focus on details
Capability to establish and maintain effective working relationships with coworkers, managers, and clients
IQVIA is a prominent global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to expanding the frontiers of human science and data science to generate the greatest possible impact – assisting our clients in creating a healthier world. Learn more at
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