TrialsConnect
A single platform that connects physicians, hospitals and sponsors to streamline trial discovery, recruitment and engagement — with clear visibility across every step of the journey.
GDPR & HIPAA compliant infrastructure
Find the right trial for your needs
Clinical trials
We help physicians, pharmaceutical companies and patient organisations make clinical trial information accessible, actionable and impactful — for every stakeholder in the research ecosystem.
Whether you're a physician, pharma team or patient organisation — we'll help you find the right setup to surface, track and act on the trials that matter most.
Explore clinical trial solutionsGive your organisation a dedicated, branded clinical trial portal — curated to your disease areas, departments or network. Patients and colleagues get a clear, trusted view of what's available, presented under your name.
A smart, localised search engine surfacing only the trials relevant to your organisation, specialty or patient population. No noise — just the studies your team and patients actually need to find.
Stay ahead of every milestone. Track the live status of trials across your department or organisation and automatically notify colleagues when a trial opens, closes or changes — so no opportunity is missed.
Turn trial data into business development opportunities. Identify active sponsors, trial sites and principal investigators in your area — giving your team the intelligence to forge the right partnerships and win more research.
Book a short, no-obligation walkthrough. We’ll show you how TrialsConnect fits your organisation and answer your questions live.
See it in action
A short walkthrough of how trial information becomes accessible, trackable and actionable for physicians, hospitals and sponsors.
For hospitals & sites
Show sponsors, referrers and colleagues exactly which studies you run, where they stand and who to contact — from one always-accurate overview.
For physicians
Matching that respects clinical reality: indication, phase, eligibility and location — so the options you see are options you can actually use.
For sponsors & CRO
Understand the competitive landscape around every indication: who is running what, where, and which sites and investigators are best positioned.
Portfolio management
One place where every study, milestone and recruitment status is tracked, so leadership and coordinators work from the same picture.
How Esperity supports trials
We work alongside sites, sponsors and patient organisations across the full arc of a study.
Trial information published in plain language inside the communities and patient organisations where people already look for answers — in their own language.
Patients and clinicians assess relevance before a site visit, so screening lists are shorter, better qualified and easier for coordinators to act on.
Structured check-ins, education and a human coach between visits keep participants oriented, informed and far less likely to disengage.
Aggregated, consented engagement and experience data that shows where the journey works — and where a protocol adds avoidable burden.
“Understanding what drives patients across their journey is key to better outcomes.”
Capabilities
Study information written for patients and published in English, Spanish, French and Dutch.
Referral overview, status and follow-up without adding another disconnected system.
Trained coaches support participants between visits, escalating clinical questions to the site.
Consented experience and adherence signals, aggregated for sponsors and research partners.
Distribution through the patient organisations that already hold community trust.
GDPR and HIPAA compliant data infrastructure with clear consent at every step.
Patient-centred by default
Every trial touchpoint we design starts from what the patient already carries: diagnosis, treatment, family and work.
Plain-language explanations of purpose, procedures and commitment.
No jargon, no pressure — patients decide with their care team.
Support in the patient’s own language, on their own schedule.
A single place to keep questions, notes and appointments together.
Evidence & trust
Esperity works with clinicians, patient organisations and research teams to generate real-world evidence alongside the trial itself — with consent, transparency and clear governance.
Next step
Bring us a protocol, an indication or an enrolment problem. We usually reply within 24 hours.
