Assistant Regulatory Coordinator

10 Week Project A clinical research site in Little Rock needs a junior regulatory professional for a 10-week contract. This is a good fit if you have some site-level regulatory experience and want to keep it current with a fast-moving team. What You'll Do Prepare and maintain regulatory binders and Investigator Site Files (ISF)Prepare and submit IRB documents, including submissions, amendments and renewalsManage essential documents and keep them audit-readyKeep study training records and logs up to dateSupport the regulatory team with document control and day-to-day admin Requirements Some hands-on site regulatory experience, ideally 1 to 2 years in clinical research at a site or CROFamiliarity with IRB submissions and essential documentsStrong organisation and attention to detailComfort with Microsoft OfficeRight to work in the US without requiring sponsorship Ability to start quickly Nice to have A two-year degree or higherPhase I experienceKnowledge of GCP