Protocol depth.
Without the hiring cycle.
A pre-vetted network of clinical development, operations, biostatistics, medical writing, and field monitoring specialists — matched to the shape of your program gap in 48 hours.
● LIVE SIGNAL · CLINICAL NETWORK
Depth. Not coverage.
Clinical Development
Protocol design through pivotal readout. Study ops, vendor strategy, functional plan orchestration.
- Protocol design & amendments
- Study operations & vendor management
- Functional plan orchestration
- IND / FIH planning through Phase 3
Biostatistics
Regulatory-grade SAPs, programming, PK/PD, survival analysis. Depth by therapeutic area.
- Statistical analysis plans
- SDTM / ADaM / TLF programming
- PK/PD & population pharmacology
- Survival & oncology endpoint analysis
Medical Writing
Protocols, CSRs, IBs, safety narratives from ex-industry writers with TA fluency.
- Protocol & protocol amendments
- Clinical study reports (CSRs)
- Investigator brochures
- Safety narratives & DSURs
Field Monitoring
4,000+ specialist CRAs across 20 countries. Risk-based monitoring, specialty therapeutic areas.
- 4,000+ vetted CRAs
- 20 countries / global deployment
- Risk-based monitoring (RBM)
- Study rescue & recovery
Three scenarios. One 48-hour promise.
Phase 1 biostat leaves mid-readout.
Lead biostat takes surprise medical leave three weeks before readout. You need a replacement inside your EDC and TLF programs fast.
Phase 3 team in 14 countries.
Scale monitoring across 14 countries in under a month. CRO can't deliver on your timeline. Hiring path is impossible.
CMO leaves six months before BLA.
You can't hire another full-time CMO in time, but the program cannot move without one.
Your clinical gap.
Closed in 48 hours.
Tell us the shape of the problem, not the job description. We return three pre-vetted specialists with therapeutic area fit.