For hospitals and departments

Your department's trials: one current view for everyone who needs it

The situationThere is no single, current overview of which trials are open in which department, who runs them, and where colleagues can refer.

TrialsConnect gives each department a shared, locally maintained view of its research: to run the trials you have, assess new ones with confidence, and make your trials and expertise easy to find. Free for every participating hospital.

Three goals, one workspace

TrialsConnect: clinical trial registries connected to hospital departments and sponsors

Manage your portfolio

Every trial, investigator and local status in one place.

Help physicians find trials

Colleagues in your hospital and network find the right study and contact.

Grow your research

Answer feasibility requests faster and show sponsors what you can do.

Department trial overview

One clear overview, kept current by your team

A shared starting point for the department head, physicians, research nurses and coordinators, for portfolio reviews and day-to-day questions.

  • Every trial preparing to open, recruiting, paused, closed to recruitment or in follow-up.
  • Responsible investigators and research contacts, disease areas, biomarkers, phases and sponsors.
  • Record local changes yourself: recruitment opening, pausing or resuming, a new contact, follow-up, or a request for sponsor confirmation.
  • Your team reviews the list, so the right trials are linked to the right people and missing studies are added.
Local status update · Trial 2Illustrative
RecruitingOn hold
Updated by
Study coordinator, oncology
Date
14 Oct
Scope
This site only
Sponsor
Confirmation requested
Every update carries its source, date and scope.

Investigator activity and workload

See who is involved in what, and when demands overlap

A physician view shows each investigator's studies, their role, the local stage of each study and the periods when responsibilities coincide.

  • Support decisions on who takes on a new study, and on investigator and co-investigator roles.
  • Plan research nurse and coordinator support for periods when several studies open or recruit at once.
  • Physicians or authorised staff keep their own profile accurate: role, specialty, experience, studies and declared research interests.
  • Profiles stay current when people join, move or change responsibilities.
Investigator activity · next 12 monthsIllustrative
RecruitingOpeningFollow-upProposed
Study counts give an overview. Workload also depends on complexity, study stage and support staff.

Feasibility and capabilities

Better-supported answers to feasibility questionnaires

When a new study is offered, compare its recruitment window with your existing and planned studies, and reuse what you already know about your department.

  • Spot studies that may recruit from similar populations, with overlapping indications, biomarkers or treatment settings.
  • Check investigator responsibilities and shared staff, diagnostic, laboratory or procedural needs in the same period.
  • Keep one capability profile: expertise, research team, laboratory and imaging, pharmacy, specialist procedures, and services from the wider hospital.
  • Answer with clear assumptions, and confirm only what is specific to the protocol.
Feasibility check · proposed biomarker studyIllustrative
  • Biomarker testing available in-house
  • Research nurse support in capability profile
  • Overlap: 2 studies recruit a similar population in the same period
  • Imaging schedule to confirm with radiology
Your capability profile answers the general questions; you focus on what is specific to the protocol.

Sponsor opportunities

Become easier to discover for relevant studies

See which sponsors are active in your disease areas, and present your department's expertise when you discuss new studies.

  • Sponsors with documented research activity in your areas, by phase and study type, in your country or region.
  • The relationships already in your own portfolio.
  • A focused capability presentation for discussions with sponsors and CROs.
  • You choose which profile and capability information is shared with sponsors.
Sponsor activity · your disease areasIllustrative
SponsorStudies in your areasWith you today
Sponsor A6 · phase II–III2 trials
Sponsor B4 · phase IIINone yet
Sponsor C3 · phase I–IINone yet
Published activity gives context; future opportunities are confirmed with the sponsor.

One update, many uses

When a coordinator updates a trial's local status, everyone who relies on it sees the same current information. That is a practical reason to keep it up to date.

Coordinator updates local statusTrial 2 · Recruiting → On hold · 14 Oct
  • Department overview
  • Investigator's profile
  • Hospital trial search
  • Overlap check for new studies
  • Reports shared with sponsors

The same goes for your capability profile: one update supports the next feasibility response, internal planning and what you choose to share with sponsors.

An example: an oncology department answers a feasibility request

  1. Check the portfolio

    The team finds existing studies that may recruit a similar biomarker population in the proposed period.

  2. Check people and resources

    It reviews investigator responsibilities and confirms the staffing and testing the new protocol needs.

  3. Reuse and ask colleagues

    It reuses its capability profile and shares a synopsis with relevant physicians to check referral pathways.

  4. Answer clearly

    The response sets out confirmed capabilities, the basis for the recruitment estimate, potential overlap and open points.

  5. Go live

    If the study proceeds, the team adds its contacts, status and documents, and colleagues can find it in the hospital search.

Value for everyone in and around the department

Department leadership

The portfolio, how research responsibilities are spread, overlapping demands, and opportunities to grow research.

Principal investigators and physicians

Their own study involvement and research profile, relevant colleagues, and trials across the institution.

Research coordinators and study nurses

Keep local status and documents current, coordinate contacts, and reuse information for feasibility responses.

Physicians across the hospital or network

Find relevant studies and reach the right research team with current information.

Sponsors you choose to share with

Your stated capabilities, investigator experience and research interests, as input for further discussion.

Independent and free

Clinical Trial Unit team meeting

Hospitals use the workspace free, directly from Esperity. No pharmaceutical company funds, selects or is linked to a hospital's access.

In return, your centre keeps its trial status current. That makes the information better for every physician who searches it.

In a pilot we measure how quickly a physician finds a relevant trial and contact, how current local status records are, the time needed for feasibility responses, reuse of capability information, and sponsor discussions that follow from shared department profiles.

Get your department workspace

Tell us which hospital and department. We pre-fill your trials before the first call.