Site Research Assistant

Responsibilities

• Provide clinical research support to investigators and site staff
• Verify and correct research study information on source documents and manage research queries
• Input research study data into Electronic Data Capture (EDC) systems while maintaining quality control
• Prepare, maintain, and compile research study files and regulatory/ethics documentation
• Maintain FDA 1572 forms for assigned research studies
• Schedule subject visits and generate necessary reports and documents for research subjects
• Input visit data into the Clinical Trial Management System (CTMS) to track patient visits and study budgets

Requirements

• Bachelor's Degree in Life Sciences or a related field
• 1 year of clinical research experience as a Study Coordinator
• Intermediate English proficiency
• Basic knowledge of clinical trials and medical terminology
• Proficiency in MS Office applications (Word, Excel, Outlook, Access)
• Ability to work onsite at the research center
• Strong attention to detail and excellent interpersonal skills

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.