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.


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


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.
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.
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.
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.
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.
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.
Explore our end-to-end, full service clinical development capabilities including Therapeutics expertise, Development Planning, Phase I early clinical development, Phase IIb/III and Phase IV Trials, Regulatory Submission and Post-Launch Studies.
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Ease the burden on your sites and make it easier and more appealing for patients to enroll and remain engaged.