Clinical Study Administrator

Role: Study Start-Up Coordinator (SSU CSA) supporting clinical trial site activation at AstraZeneca. Responsibilities: coordinate and administer site selection through activation, ensure accurate tracking, review startup documents per ICH-GCP and local regulations, support regulatory submission and site readiness, attend study meetings, and maintain tracking systems. Requirements: high school diploma or GED; 1-3 years in clinical research or regulated administrative roles; strong organizational, communication, and computer skills; proficiency in English. Preferred: degree in Life Sciences or Healthcare; experience with clinical trial start-up processes, vendor management, and familiarity with systems like Veeva or Box; ability to develop advanced computer skills and work in an international team. High-Value: entry-level role in clinical trial operations, supporting AstraZeneca’s regulated studies, with a focus on study start-up activities. Work setup: not specified, likely office-based; no travel requirements stated.