For research sites and startup teams

Clinical Trial Site Activation Software

TrialConnx gives research site leaders and startup, regulatory, and contracts teams one live status across every study, so you catch stalls early and activate faster.

What changes

Stop chasing status. See the stall.

You already know the work. TrialConnx takes it off email and spreadsheets and puts stage, owner, and aging in one place.

Status in inboxes

BeforeToday you rebuild where a study sits from email, spreadsheets, and the last person who replied.
With TrialConnxTrialConnx keeps stage, owner, and a record of what changed on the study, so the next update is the record.

Stalls found too late

BeforeBudget, contract, and IRB work sits with someone for days, and leadership hears about it when a meeting asks.
With TrialConnxTrialConnx shows aging and studies stuck longer than 30 days, so you act before the status call.

No view across studies

BeforeCoordinators, regulatory, contracts, and leadership each keep a different list.
With TrialConnxTrialConnx is one live status across every study, for the people getting it ready to enroll.

What you stop doing by hand

TrialConnx tracks the work at each stage

The stages are how TrialConnx follows the study. You stop hunting the status.

1

Intake

The request is on the study, not only in an inbox.

2

Feasibility

Fit, capacity, and the decision stay with the study instead of in a side email.

3

Budget

Coverage and cost stay with the study, not in a spreadsheet beside it.

4

Contract

You see who has the next contract edit, so the chase is one look, not another email.

5

IRB

You see whether it is submitted, how many rounds of changes it has had, and how long it has been sitting. TrialConnx does not replace your IRB portal.

6

Activation

Everyone can see when the study is ready to enroll. Your CTMS stays in place for enrollment and day-to-day trial management.

Stage on every study

Intake through activation, on every open study.

Who owns the next action

Site, sponsor or CRO, PI or department, IRB, or contracts.

How long work has been waiting

Including studies stuck longer than 30 days.

A record of what changed

Status is not rebuilt from the last email.

Proof from one cancer center

Faster activation, once the work was visible

At one anonymized NCI-designated cancer center, activation fell from about 120 to 99 days after two process changes.

The window
60%
Of the 120-day window
Went to waiting, one step after another, before budget work could begin.
21
Days saved per study, within the first 30 days of visibility, without added headcount or rewritten procedures.
120 to 99
About 120 days before, about 99 days after.
2
Changes. Starting the budget sooner, and moving the Resource Meeting so the work overlapped.

Full narrative: AMC activation case study.

The day's work

Documents, budget, contract, and IRB stay on the study

TrialConnx is where coordinators run the work of getting a study ready. Each piece has an owner and a due date, so the next step is on the study, not in a side inbox.

Documents

Regulatory documents are collected on the study. You see what is ready and what is still out, including the packet an IRB submission is waiting on.

Budget and contract

Coverage, cost, and the contract live on the study. TrialConnx shows who has the next contract edit, and the date that work is due.

IRB

Follow each submission from the documents being ready, through its status and each round of changes, to how long approval is taking.

Owner and due date

Open activities list the person and the date. Coordinators see what is past due before someone has to ask in a meeting.

The sponsor update

The sponsor sees the same picture the site already has

Site directors and PIs do not wait for someone to build a report. The note you send the sponsor starts from that picture, so email is not a second place to keep status.

What is in the picture

Where the study stands, what is blocking it, who owns the next step, and which dates are at risk.

What drops off the week

The round of emails that used to rebuild status before you could answer the sponsor.

Your CTMS

TrialConnx integrates with the CTMS your site already uses

OnCore, Veeva, Medidata, WCG, RealTime, or a CTMS your team built. TrialConnx runs the opening of the study beside it. When the site is ready to enroll, that startup record moves into the CTMS.

Study details

Study number, sponsor, PI, and the site, captured while the team was getting the study ready.

Budget and contract

The approved budget, and where the contract landed, move with the study.

IRB and ready to enroll

Submission status, the approval, and the point the site is ready to open move across too.

The same handoff, spelled out: Study startup vs CTMS.

FAQ

Questions site teams ask

Where do coordinators keep documents while a study is opening?

On the study in TrialConnx. Regulatory documents are collected there, and you can see what is ready and what an IRB packet is still waiting on.

Who has the budget or the contract right now?

Both live on the study. TrialConnx shows who has the next edit and the date that work is due, so the answer is not a hunt through email.

How do we follow an IRB submission across our studies?

Each submission shows document readiness, current status, each round of changes, and how long approval is taking. One that is at risk of slipping shows up before it holds the study.

How do we answer the sponsor without rebuilding status in email?

Directors, PIs, and the sponsor see the same picture: where the study stands, what is blocking it, who owns the next step, and which dates are late. The note you send starts from that picture.

What does our CTMS receive when a study is ready to enroll?

TrialConnx integrates with the CTMS you already use. Study details, the approved budget and contract status, the IRB status, and the ready-to-enroll mark move into that system.

What does a site director see across every open study?

One picture of every study still opening: stage, what is blocking it, who owns the next step, and which dates are at risk, including studies sitting longer than 30 days. Leaders see it without waiting for a report to be built.

Bring the studies your coordinators are opening.

We will walk the documents, the budget, the contract, the IRB, and the move into your CTMS.