Entry Level Life Sciences Hiring Event - September 15th

Validate entry database designs, report metrics, and identify data conflicts for Clinical Data Coordinators. Monitor sites independently, travel 60-80% of the time, and communicate with medical staff for Clinical Research Associates. Coordinate daily study activities, maintain project timelines, and serve as the central contact for Project Coordinators. Collect essential site documents, perform quality reviews within the Trial Master File, and assemble regulatory submissions for Regulatory Submissions Coordinators. Perform documentation, routine lab operations, and troubleshoot automated instrumentation for Medical Technologists.