Clinical Trials Documentation Specialist - IRB & CTMS

A leading molecular science company in Arizona is looking for a Clinical Study Documentation Specialist to support clinical trials and ensure compliance with regulatory requirements. Responsibilities include preparing IRB submissions, maintaining study documents, and collaborating with research sites. Candidates should have an Associates degree, two years' experience with IRBs, and strong organizational skills. It offers an opportunity to contribute to transformative cancer treatment innovations within a mission-driven environment. #J-18808-Ljbffr