IP Administration Program Lead Investigational Products
Listed on 2026-09-22
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IT/Tech
IQVIA is seeking a Site Investigational Product Specialist (SIPS) to lead the IPPI administration in clinical trials, ensuring safe and efficient drug handling and comprehensive training across investigational sites.
You will co-author IPPI documentation, develop training materials, and act as the primary interface for site teams and trial staff. The role requires nursing leadership, trial experience, and strong communication skills to ensure compliance with SOPs and ICH/GCP guidelines.
Consider building your career as a IP Administration Program Lead for Investigational Products at IQVIA.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in NC, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, IT & Technology.
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