At first glance, it looks like a paradox: pharma companies pour billions into AI pilots, and yet the success stories are rare. Why? Because AI is not magic—it magnifies the cracks in your data, trust, and operating model.
Veeva’s 2025 report, The State of Data, Analytics and AI in Commercial Biopharma, nails the pain. Among senior life sciences leaders: 89% say they couldn’t scale more than half of their AI initiatives, 96% claim their data isn’t structured or AI-ready, and 67% have abandoned AI projects due to foundational data issues. One painful impact: fragmented HCP/HCO data has caused two-month launch delays and 15 % lower early script volume.
Those numbers aren’t rock-solid alone, but they align with what’s happening in other industries. For example, a recent MIT report found that while 95% of enterprise AI pilots fail to deliver measurable ROI, the gap isn’t about model quality — it’s about approach. The few that succeed do so by embedding AI into real workflows, tailoring it to specific business processes, and using feedback loops to learn and adapt over time.
The Root Tension: Model vs. Foundation
The temptation is always to blame the model: “Our algorithm didn’t generalize.” But that’s rarely the first or biggest failure. The real failure starts deeper:
Trust is the first casualty
Even a technically excellent prediction is useless if field users don’t trust it. In pharma, trust fractures when the data basis is inconsistent: duplicate HCPs, misaligned specialties, stale affiliation updates. The moment a rep or MSL sees something obviously wrong, they stop believing the system.
A recent systematic review, From Challenges and Pitfalls to Recommendations, notes that many federated learning efforts in healthcare still struggle with bias, non-IID data, and communication overhead — issues that undermine the reliability and trustworthiness of their results.
When insights arrive too late
Pharma is fast-moving. If your AI signals arrive after the field has already called or after the window has closed, they’re useless. Veeva reports that some teams spend up to 100 days just cleaning or matching HCP data, and up to 200 days navigating access contracts before insight generation can begin. That’s latency in action.
Architectures like federated learning help reduce data movement latencies. The MDPI review of FL points out that in healthcare settings, FL enables decentralized model training without sharing raw data, which can avoid bottlenecks.
But that speed comes with trade-offs: communication overhead, synchronization, and non-IID node divergences slow things down in practice.
Consistency is the silent killer
Global pharma operates in many markets, each with local conventions, vendor taxonomies, and mappings. Veeva indicates that nearly all companies repeatedly map and remap global-to-local specialty codes, investing significant annual effort in HCP mapping.
Even in FL literature, heterogeneity is a recurring challenge. The Federated Learning in Healthcare: Model Misconducts, Security, Challenges review describes how differences across data silos—bias, variations in labels, missing features—can degrade global model performance.
So the harsh truth: a federated model built on inconsistent or poorly mapped data is only as good as the weakest node.
But Wait — There Are Counterpoints
I don’t believe in a single narrative of doom. There are successes, contradictions, and caveats worth exploring.
- According to MIT’s 2025 report, while 95% of organizations realize no measurable ROI from GenAI pilots, 5% achieve significant financial impact. The difference isn’t model quality—it’s learning and workflow integration. Successful pilots align AI to specific processes, adapt over time, and embed feedback loops to improve continuously.
- FL is not just academic hype. Recent methodological advances show new protocols for aggregation, privacy, personalization, and fairness. These improvements hint that FL may become viable for health/clinical use soon.
- Some organizations partially centralize or use hybrid architectures: centralizing non-sensitive metadata, keeping patient-level data local, and merging insights at a higher level. This hybrid path is underexplored—but offers a pragmatic middle ground when pure FL is too fragile.
- FL has its own risks: privacy attacks, fairness distortions, auditability challenges. The “From Challenges and Pitfalls” review is blunt: many FL models are not currently suited for high-stakes clinical use unless rigorous safeguards are in place.
What This Means for Medical Affairs & Commercial
If your goal is reliable, scalable AI in pharma, do not build from the rear. Focus on foundation.
Co-own identity, mapping, and lineage
Medical affairs and commercial must agree on a shared gold standard for HCP/HCO identity, affiliations, specialties. Local nuance is allowed—but divergence cannot be. Make reconciliation, version control, and audit trails your first project.
Treat readiness as a gate, not a checkpoint
No AI use case proceeds unless basic readiness criteria are met: % mapped entities, data freshness, lineage completeness. That “no readiness, no run” posture is how you avoid building on sand.
Use federated / hybrid cautiously
FL and hybrid designs have power—but only when nodes are aligned, data is reasonably clean, and governance is strong. Use lessons from FL reviews (communication cost, bias, auditability) to choose your architecture.
Show your work to the field
Build explainability, error flags, and feedback loops from day one. The moment a rep sees a wrong call, you lose adoption—and with it, ROI.
Start narrow, then widen
Begin with cross-domain use cases you jointly own (MA + Commercial). Reuse your identity and pipeline infrastructure. Expand only after demonstrating trust, speed, and consistency in one domain.
Conclusion: Scaling Trust Before Scaling AI
Pharma’s AI paradox isn’t about technology underperforming; it’s about organizations overestimating their readiness. Both Veeva’s data and MIT’s analysis converge on the same insight: most pilots fail not because models are weak, but because foundations are. The winners don’t simply deploy smarter algorithms—they build environments where data is trusted, context is consistent, and feedback loops are real.
Federated learning may one day solve pieces of the privacy and access puzzle, but even the most elegant architecture can’t compensate for internal misalignment. Bias, latency, and heterogeneity aren’t coding errors—they’re organizational ones. And as long as Medical Affairs and Commercial run on separate definitions of truth, AI will only automate confusion at scale.
The path forward is uncomfortable but clear: go slower to go faster. Harmonize identity, prove readiness, and earn trust before automating decisions. Prioritize interoperability and explainability over novelty. Build a system where every insight can answer not just what it predicts, but why.
Pharma’s next frontier in AI isn’t intelligence—it’s integrity. The companies that internalize that distinction will stop running pilots and start leading transformations.
Moe Alsumidaie is Chief Editor of The Clinical Trial Vanguard. Moe holds decades of experience in the clinical trials industry. Moe also serves as Head of Research at CliniBiz and Chief Data Scientist at Annex Clinical Corporation.



