iconplc - United States, IT - Administration, Hybrid work

Join ICON plc as a Clinical Study Specialist in Basking Ridge, NJ, supporting global trials across NA, LAM, EU, APAC, and India. Leverage your TMF, CTMS, and SharePoint expertise to organize reports, coordinate meetings, and review study documents. Requires a Bachelor’s degree and 2+ years of ind...

Clinical Study Specialist role at ICON plc, a global leader in clinical research. Based in Warren NJ, Armonk NY, or Cambridge MA (hybrid). Requires a Bachelor’s degree and 2+ years industry experience supporting global trials with TMF, CTMS, and SharePoint. Enjoy competitive benefits, annual leav...

Join ICON plc as a Senior Validation Engineer in Blue Bell, PA or Raleigh, NC. This office-based role with remote flexibility requires 10+ years of CSV/GxP experience. You will lead validation for complex global projects, ensuring compliance with FDA and EMA regulations. We offer competitive heal...

Join ICON plc, a global clinical research leader, as a Set Up Specialist. You will coordinate clinical trial setup, ensuring regulatory compliance and efficient study execution. This role requires a life sciences degree and experience in trial setup or site management. The position offers competi...

Join ICON in San Antonio as a CMC Project Manager I. You will lead CMC projects for early-phase drug development, ensuring GMP compliance and coordinating cross-functional teams. This role requires 1+ years of project management experience in a pharmaceutical setting. We offer competitive health ...

Join ICON plc, a global clinical research leader, as a Project Manager I EDS. This hybrid role in Whitesboro, NY requires 3+ years of lab or project management experience. You will manage bioanalytical project timelines, budgets, and client coordination. We offer competitive health insurance, ret...