The Celéri Research Group doesn't deliver a fixed bundle of services — it delivers the right combination of best-in-class partners for what your study actually needs. From CRO services and biostatistics to EDC infrastructure, QMS systems, behavioral science, and reputation building — we curate the team around the objective, not the other way around.
Most CRO relationships lock you into a single firm's capabilities — and you pay for everything they offer, whether you need it or not. The Celéri Research Group works differently.
We maintain relationships with best-in-class specialist partners across every dimension of clinical research — and we assemble the right combination for your specific study, stage, and budget. Sponsors and investigator-researchers get access to capabilities that would typically require multiple separate vendor relationships, coordinated through a single point of contact.
You contract only for what you need. As your study evolves, the partner mix evolves with it.
The Research Group supports two distinct engagement types — each drawing from the same curated partner network, scoped differently.
If you're exploring investigator-initiated research, studies, or trials — we can help from day one. We assist with optimal study design, electronic data capture, PRO development, and site management — with access to over 350 pain network providers and AI-based patient recruitment.
We support the full trial spectrum — IDE through post-market studies — for sponsors who need advanced evidence infrastructure for their device or therapeutic. Our depth of clinical registry experience delivers irrefutable data and insights for RWD requirements, regulatory submissions, and payer access.
Celéri doesn't maintain one vendor relationship for every capability — we curate specialist partners who are genuinely best-in-class in their domain. Named partners below represent the core of the network.
Purpose-built EDC and quality management systems for regulated clinical research. Greenlight Guru Clinical brings a study management platform designed specifically for medical device trials — not adapted from pharma or academic research tools.
Greenlight Guru ClinicalExperienced clinical research operations — site management, regulatory strategy, monitoring, and data management — delivered by a firm that understands the specific demands of interventional pain and neuromodulation studies. Fit-to-purpose: not a large firm when a boutique delivers better results.
Hart Clinical ConsultantsBuilding clinical credibility requires more than publication — it requires strategic communication, KOL positioning, and a narrative that translates evidence into market impact. Feed brings healthcare marketing and scientific reputation capabilities that most CRO relationships simply don't include.
Feed, The AgencyRigorous biostatistical design, power calculations, interim analysis, and publication-ready outputs — paired with HEOR modeling for payer dossier development. Right-sized to your study: boutique firms for focused analyses, larger partnerships for complex multi-site datasets.
Hart Clinical ConsultantsCompletion rates, retention, and the quality of PRO data are behavioral problems as much as operational ones. Celéri's behavioral science partners inform outreach sequence design, consent communication, and longitudinal engagement strategies — the reason our registry completion rates exceed industry averages.
Hart Clinical ConsultantsFrom clinical study reports and regulatory submissions to peer-reviewed manuscripts and congress abstracts — medical writing partners who understand pain, neuromodulation, and the publication standards that matter to the journals your data belongs in.
Network PartnersAny individual partner on this list is excellent at what they do. What Celéri provides is the judgment to know which combination is right for your study — and the relationships to activate them quickly. We've seen what happens when a sponsor brings in the wrong CRO size, the wrong EDC system, or skips the behavioral science layer entirely. The Research Group exists to prevent that.
The Research Group can engage across any combination of the following capabilities — scoped to your study, your stage, and your budget.
Boutique or larger firm — matched to your study's scale and complexity
Study design, power calculations, interim analysis, publication-ready outputs
Small, medium, and large — including Greenlight Guru Clinical for device studies
Quality management systems purpose-built for regulated medical device research
FDA strategy, IDE applications, PMA supplements, 510(k) support
Remote and on-site monitoring, data verification, GCP compliance
Patient engagement design, retention strategy, outreach optimization
Key opinion leader mapping, engagement strategy, advisory board support
Clinical study reports, manuscripts, abstracts, regulatory documents
Scientific communications, healthcare marketing, evidence-to-market narrative
Database design, data cleaning, audit trails, regulatory-grade data stewardship
AI-based matching across the Celéri pain network — 350+ providers, PatientFinder™ technology
Whether you're designing your first investigator-initiated study or managing a multi-site sponsor trial — the Celéri Research Group will identify the right partner combination and get your study moving.