IQVIA Flex Outsourcing Solutions

Ready for a truly custom approach to your trials?

Partner with us to customize the optimal blend of IQVIA’s full service and FSP delivery models to meet your specific requirements.

Partnering to blend the optimal FSP & FSO clinical trial outsourcing solutions customized to your needs

Solutions tailored to your needs

Flex Outsourcing Solutions offers you the agility & flexibility to meet any requirements and utilize either IQVIA systems & SOPs—or stay within your in-house systems.  Scalable to your needs, we create custom solutions that can support needs at a project, asset, or the portfolio level.

Streamlined customer service

Your single point of contact—an IQVIA Delivery Lead—is accountable for overseeing & coordinating your customized IQVIA delivery team. You can be assured of simple, streamlined communications that significantly eases your oversight burden.

Implementation and rapid deployment

Dedicated implementation team and rapid deployment of resources and capabilities to meet accelerated milestones with the agility to adjust over time. At the same time, IQVIA helps ensure effective change management that facilitates a rapid transition to your new model.

Optimized transparency & visibility

IQVIA Flex Outsourcing Solutions creates a customized oversight model to enable operational transparency and data visibility. We also partner with you to align on the optimal KPIs and reporting cadence.

Unparalleled expertise

Our vast wealth of institutional knowledge, data, experience, and innovative solutions makes IQVIA your clear choice for combining & customizing the optimal FSP and FSO solutions.

Maximize clinical trial outsourcing customization by leveraging Connected Intelligence™

By connecting IQVIA’s long track record of success and innovation in trial management with the integration of our tech-enabled solutions, optimal collaboration, and streamlined communications, you can be assured of tailoring the optimal mix of full service & FSP solutions to meet the needs of your clinical trial.

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