Teams at Premier Research

Perform central monitoring of clinical trial data using eCRF and ePremier visualization tools to assess data quality, patient safety, and site performance. Develop risk analytics and monitoring plans, present findings to sponsors and internal teams, guide site monitors, escalate issues, and document corrective actions to ensure compliant, timely trial execution.

The Sr/Site Start up Associate II prepares and submits regulatory applications, negotiates site contracts, ensures compliance, and guides clinical trial processes.

As a Software Quality Analyst, you will execute testing, apply software test methodology, validate compliance, conduct unit testing, and handle various assignments.