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.
Delivery decisions global health teams are forced to make
Global health R&D organisations face distinct challenges that can limit their ability to deliver impact:
Our approach is based on deliberate delivery choices
We choose embedded delivery over episodic outsourcing, because sustainability and trust matter more than short‑term efficiency. View our video series on how we are helping to reshape global health.
How we design partnerships for mission‑driven delivery
In global health, partnership models matter as much as scientific ambition. IQVIA designs partnerships that prioritize durability, local ownership, and accountability — because mission‑driven work operates under constraints standard outsourcing models were not built for.
Mission‑driven delivery requires partnerships that make trade‑offs explicit — and design for them upfront. See how IQVIA structures partnerships that survive changing timelines, funding cycles, and governance demands. Link to video: https://bcove.video/4ucn8xx
Applied across low‑ and middle‑income settings through long‑standing global health partnerships.
We have learned how to do capacity building without creating dependency — and we design for sustainability from day one. Watch the video to hear from our local teams in Africa. Link to video: https://bcove.video/4rOEkYp
IQVIA offers highly adaptable delivery models designed to meet the evolving needs of non‑profit and global health organisations.
This includes:
Proven across global health partnerships, non‑profits, and mission‑led programmes worldwide.
View the video to hear directly from our operational experts. Link to video: https://bcove.video/3OPWaM5
By combining flexible engagement models, embedded local capability, and scientific rigor, IQVIA enables mission‑driven organisations to deliver impact at scale without losing control or sustainability.
Proven through long‑standing partnerships supporting global health research, development, and delivery worldwide. Watch the video to hear from our global health experts. Link to video https://bcove.video/4t5h0p4
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.