Associate Study Coordinator-ISR

Coordinate study tasks from pre-study initiation to completion by assisting Study Directors and Principal Investigators with planning, protocol generation, and data collection. Manage pre-clinical data entry, documentation, and analysis while maintaining facility SOPs and accurate client inventory. Support test/control article accountability, distribute study documents, and ship specimens with proper chain of custody. Communicate progress to Sponsors, facility management, and internal teams, and assist in generating technical reports and identifying issues. Perform special projects including data tabulation, correspondence, and routine updates to support daily operations.