Translational pain science & trial strategy

Smarter decisions for pain & analgesia programs.

NociWise — Pain Translation & Strategy

NociWise helps biotech, CROs, and clinical teams de-risk pain programs by tightening the chain from target and mechanism to models, biomarkers, endpoints, and go/no-go decisions.

Domain: nociwise.com · Remote-friendly from Dallas–Fort Worth, TX

Services

What NociWise does

NociWise combines deep pain neurobiology with pragmatic trial and program design—so your team gets clearer signals, tighter rationale, and cleaner decisions.

Translational Program Strategy

From mechanism to go/no-go

Align targets, models, biomarkers, and endpoints into a coherent translational narrative that stands up to investor, internal, and regulatory scrutiny.

Target & indication mapping Model & assay selection Evidence roadmap

Pain Trial Protocol Review

Endpoint & signal optimization

Stress-test your protocol for feasibility, noise, and credibility: inclusion/exclusion, endpoints, measurement schedules, and operational risks.

  • Endpoint hierarchy and timing
  • Confounds and bias control
  • Recruitment & burden review

Biomarker & Assay Planning

Mechanism-linked readouts

Design biomarker and assay strategies that reflect the biology of your program and support translational claims.

Mechanism-tied markers Assay feasibility Sampling & analysis logic
Packages

Structured, outcome-focused engagements

Each package is scoped around specific deliverables and timelines. Pricing is tailored to complexity and urgency.

Translational De-Risk Sprint

10–14 days · fixed scope

Tighten your pain/analgesia program from mechanism to decision gates.

  • Target–indication–patient mapping
  • Preclinical model & endpoint strategy
  • Biomarker & assay outline
  • Go/no-go and risk register

Ideal before major internal reviews, financing, or partnering discussions.

Protocol & Endpoint Audit

5–10 days · one-time review

A focused scientific and operational review of a pain trial protocol.

  • Annotated protocol with comments
  • Endpoint and schedule critique
  • Signal/noise and feasibility assessment
  • Priority recommendations list

Works well for sponsor, CRO, and academic-led pain trials.

Data → Figures → Story Sprint

5–12 days · dataset-based

Turn complex experimental data into clear figures and a coherent scientific narrative.

  • Clean analysis outputs and plots
  • Publication-ready figure layouts
  • Results text and figure legends
  • Reproducibility and file-structure notes

For internal decks, manuscripts, or partnering materials.

Retainer-based advisory support (e.g., monthly office hours and ad hoc reviews) is available for select teams. Contact us to discuss fit and availability.

About

Scientific depth, practical execution

NociWise is led by a translational pain scientist with postdoctoral experience in anesthesiology and pain management, combining mechanistic insight with hands-on work in models, assays, and analysis.

Scientific background

Expertise across pain neurobiology, nociceptor signaling, and translational models, including:

  • GPCR / cAMP signaling and ion-channel modulation
  • DRG neurons and pain-relevant cell models
  • qPCR, RNAseq, and molecular readouts
  • Behavioral and functional pain endpoints

How we work

Every engagement is built around:

  • Evidence-first recommendations
  • Clear assumptions & limitations
  • Practical next steps for your team
  • Transparent documentation

Who we serve

NociWise typically partners with:

  • Biotech teams building or refining pain programs
  • CRO project leaders seeking specialized input
  • Academic investigators designing pain studies

If you work in nociception, analgesia, or pain-related targets, NociWise can help sharpen the path from data to decision.

Contact

Discuss your program or trial

Share a brief overview of your program, where you are in development, and what decisions are coming up. You’ll receive a short reply outlining whether and how NociWise can help.

Get in touch

Email: hello@nociwise.com

Location: Dallas–Fort Worth, Texas (remote-friendly)

Typical response time: 2–3 business days. Please avoid including confidential or patient-identifying information in your initial note.

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Disclaimer: NociWise provides scientific and strategic consulting services only. It does not offer medical care, diagnosis, treatment recommendations for individual patients, or legal advice. Any consulting work is subject to applicable institutional conflict-of-interest and outside-activity policies.