Agentic AI · Life Sciences Expertise
LynQX is an agentic-AI marketplace connecting pharma, biotech, investors, and recruiters with credentialed life-sciences experts — at consumer-software speed, with the rigor regulated work demands.
Powering expertise discovery across
Every credential verified against authoritative public sources
The problem
Drug discovery in 2026 demands depth: regulatory CMC, adaptive Phase 2 design, AAV manufacturing scale-up, GxP-validated AI. Generic talent platforms can't read it.
A computational biologist's 7-year depth in CAR-T translational research disappears when reduced to job titles on a CV.
A talent partner can't tell whether "Phase 1/2 oncology" was protocol design, regulatory authorship, trial execution, or biostatistics.
Biotechs need fractional CSOs, advisory CMCs, SAB members for projects — the market assumes fractional means junior or low-commitment.
AlphaFold-fluent engineers, generative chemistry specialists, GxP-validated data scientists don't surface in keyword searches.
Who actually delivered on a hard program is locked inside each sponsor. There's no shared signal of proven, verified performance to source from.
Who LynQX serves
The same network of credentialed life-sciences experts, presented for the workflow that fits your role.
Featured engagement types
Verified KOLs across oncology, gene therapy, neurology and beyond. COI screening + automated rotation reminders.
Senior life-sciences leaders working 4–16 hrs/month. Tier-3 verified. Negotiator handles outreach, scheduling, and NDA flows.
Fixed-fee or hourly projects with kanban applicant pipelines, milestone-triggered payouts, and immutable IP assignment chain.
Verifier + Compliance Sentinel + Insight Synthesizer in parallel. PDF + structured JSON, with a source link under every fact and an explicit gap wherever LynQX holds no evidence.
How it works
The work that takes recruiting partners weeks happens continuously in the background. You decide what to do with it.
Type a need in natural language — "Phase 2 oncology PI in Boston with CDMO experience." Concierge translates it into structured criteria.
Matchmaker traverses the capability graph (publications, trials, patents, MeSH terms) plus vector similarity, ranks the top N with reasoning.
Verifier confirms credentials with audit-grade sources. Compliance Sentinel runs debarment + COI in parallel. You approve or override.
Negotiator drafts outreach + scheduling + NDA flows. Project Operator handles timesheets, milestones, IP assignment, invoicing.
The community
Behind every Tier-2 badge is a verified professional whose credentials we can trace to the licensing board, peer-reviewed publication, or trial registration. Behind every match is reasoning you can audit.
The roster
Each agent has a single goal, scoped tools with Zod schemas, eval gates on every PR, and a human checkpoint where it matters.
Concierge
syncPersona-aware front door — every message routes here
Profiler
asyncBuilds Skills × Insights × Tools × Experience profiles
Verifier
asyncIndependent credential confirmation — Tiers 1, 2, 3
Matchmaker
syncGraph + vector hybrid retrieval; <3s ranked shortlists
Scout
asyncDiscovers experts in the wild from PubMed, NIH, USPTO
Negotiator
asyncDrafts outreach, NDAs, scheduling — humans send
Compliance Sentinel
syncSync gate on every regulated op — p95 <100ms
Knowledge Curator
asyncCaptures tacit decision knowledge from senior experts
Project Operator
asyncTimesheets, invoices, milestones, IP chain
Insight Synthesizer
asyncHeatmaps, capability gaps, salary intelligence
Trust & compliance
Compliance is not a flag we add later. It’s three layers of tenant isolation proven by a CI job, a cryptographic audit chain, agent-level data scrubbing, and an approval gate on every external side effect.
HIPAA-ready
Workspace-level toggle. The Compliance Sentinel blocks PHI access outside a HIPAA-mode workspace and requires a recorded justification; PHI never reaches an LLM.
GDPR-compliant
EU-only data residency on the EU plan. Right-to-erasure, DSR endpoints, DPA on file with every vendor.
21 CFR Part 11
Append-only audit log with cryptographic hash chain. E-signatures. Validated systems package (Phase 3).
GxP mode
Workspace toggle for clinical-trial work. Stricter compliance gates and audit retention.
Provenance, always
Every fact in the UI carries a source URL. Unattributed facts fail review. Non-negotiable.
SOC 2
roadmapNot yet certified and no observation window has started. The controls above are the groundwork; /security lists exactly what is and is not in force.
The fastest path from need to first qualified response is a conversation with our team.