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IQVIA Site Suite

Clinical trial site management and payments, from planning through archive, with investigator portals and electronic trial master files.

Solution by IQVIA
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Overview

IQVIA Site Suite is a set of digital tools designed for clinical trial sponsors and investigative sites, forming part of IQVIA's Orchestrated Clinical Trials (OCT) technology portfolio. The suite is intended to increase transparency, improve communications, and reduce the administrative burden associated with running clinical trials from planning through to archive. It is aimed at sponsors seeking to become a preferred partner for high-performing sites, run more efficient trials, pay investigative sites faster, and manage trial master files throughout the trial lifecycle.

The Site Suite brings together three core products — Clinical Trial Payments, Investigator Site Portal, and eTMF — which can each be used independently but are designed to work together to improve patient safety, reduce trial risk and cost, and accelerate time to market.

Core Products

  • Clinical Trial Payments: Supports faster payment to investigative sites, reducing financial administrative burden and improving site relationships.
  • Investigator Site Portal: Provides a centralised portal for investigative sites to access trial information, improving communication and reducing site-level administrative tasks.
  • eTMF (Electronic Trial Master File): Manages trial master files from the planning phase through to archive, supporting regulatory compliance and document management across the trial lifecycle.

Key Capabilities and Goals

  • Helps sponsors become a preferred choice for high-performing investigative sites by improving site experience and reducing administrative friction.
  • Supports more efficient and effective clinical trial execution by connecting site-facing tools and processes.
  • Improves patient safety by reducing trial risk through better site management and documentation practices.
  • Reduces overall trial cost and supports faster time to market for new therapies.
  • Manages trial master file documentation from initial planning through final archive, supporting inspection readiness and regulatory compliance.
  • Facilitates faster payment processing to investigative sites, helping to maintain site engagement and financial transparency.

Integration and Deployment Context

  • Site Suite is part of IQVIA's broader Orchestrated Clinical Trials (OCT) technology framework, which connects data, technology, and analytics across the clinical trial process.
  • The individual products within the suite — Clinical Trial Payments, Investigator Site Portal, and eTMF — are designed to function both as standalone tools and as an integrated suite.
  • Site Suite sits alongside other IQVIA clinical technology offerings including the Patient Suite, Clinical Trial Financial Suite, and Planning Suite, enabling broader integration across trial operations.

Site Suite is positioned within IQVIA's Technologies division and is available as part of the company's wider clinical trial technology ecosystem, which also includes AI-enabled tools and partner programmes supporting life sciences organisations globally.

Meta

Domain
Clinical Trial Management
Subdomain
Clinical Trial Management Systems (CTMS) & eTMF
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechCRO
Development stage(s)
Clinical
Target user(s)
QA / Regulatory AffairsClinical / Diagnostic ProfessionalIT / Systems Admin / Data Engineer
Compliance standard(s)
21 CFR Part 11GxP