Clinical Research Regulatory Specialist - SMS-3831
Springfield, Illinois, United States
$44k-$48k/yrOnsiteFull Time
SIU Medicine: Provides medical education and clinical healthcare services.
Bachelor's degree required; support clinical research operations, regulatory submissions, IRB and FDA compliance, maintain regulatory files and databases, perform QA and patient data collection.
Microsoft Access, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, eREG
Carle Health: Integrated healthcare system providing hospital services and health insurance.
Coordinate and maintain regulatory/IRB/HIPAA documents, perform informed consent review, support audits and sponsor visits; CCRP within 3 years and related bachelor's or equivalent experience.
Carle Health: Integrated healthcare system providing hospital and clinical services.
Experience with clinical research regulatory processes, IRB/HIPAA compliance, informed consent review, CITI training, and CCRP certification within 3 years; bachelor's degree or equivalent experience in a related field.