Conveloq
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Online Research Platform
We connect researchers and participants
The full-lifecycle online research platform for researchers in Asia
Which are you?

Join university research,
made easy

Browse and join online studies run by university and research labs. Find studies that match your profile, and see how to participate and what you'll be paid.

Browse open studies Log in / Sign up
Are you a participant?

Here's what's guaranteed when you join a study

✓
See open spots and deadlines up front
Know the competition and how close the deadline is before you apply
✓
Your reward is confirmed the moment you finish
Check your payout status anytime on My Page
✓
IRB approval or exemption status is always shown
Displayed on every study so you can decide to join with confidence
✓
Your personal data is pseudonymized
Your real name is never shared with researchers
See studies recruiting now →
Are you a researcher?

Register one study and the documents you need at every stage are generated automatically

01 Register your study
02 IRB documents issued automatically
Recruitment noticeStudy info & consent form
03 Recruitment & participation
Online consent recordsApplicant/completion roster
04 Settlement
Per-study settlement statement
View all issued documents →
Here's how the platform is running right now(pilot)
0
Studies registered
0+
Members
0
Completed participations
₩0
Avg. hourly rate per study
About the service

Conveloq is a platform that runs your entire study
the moment you register it

From participant recruitment to Bioethics Act consent procedures and grant settlement evidence — everything researchers used to handle piecemeal is processed through one standardized workflow. For participants, it means choosing only studies you can trust, and getting reliably compensated for your time.

1
Recruitment
Recruit participants who match your criteria, and track applications and deadlines in real time.
2
Compliance
Consent procedures under the Bioethics Act and IRB submission documents are assembled automatically in standard form.
3
Settlement
Handle participant reward payouts and grant settlement evidence in one place.
Researchers from fields like these are recruiting participants
University Psychology Depts. Behavioral Econ Labs Cognitive Science Institutes
Why it's safe to participate

Here's how your time and personal data are protected

IRB status is clearly shown on every study
Studies subject to the Bioethics Act are only posted after IRB approval or a confirmed exemption. Surveys that don't require review still show their status on the detail page.
You can withdraw at any time
Change your mind mid-study and you can withdraw consent at any time — the record is safely kept and handled with no penalty to you.
Your info is shared only under a pseudonym
Personal data is stored encrypted, and researchers only ever see a pseudonymous ID — never your real name.
Why researchers trust the platform

From precise recruitment design to Bioethics Act compliance, the platform has you covered

Screening & automatic filtering
Pre-screening questions filter out applicants who don't meet your criteria, and duplicate participation, abnormal response times, drop-outs, and failed attention checks are tracked automatically to manage participant quality.
Multi-dimensional quotas
Set up to 10 dimensions at once — gender, age, region, occupation, and more — to build your target sample.
Longitudinal (multi-session) support
Choose automatic or manual opening for each session, and freely mix online and offline sessions.
Compliant with Bioethics Act Article 16
Consent procedures are automatically assembled with all 10 required items — purpose, risk, benefit, data protection, and more — kept identical to your reviewed text.
Tamper-proof consent records
The full consent text is stored in an append-only audit log with a SHA-256 hash, ready to hand over for closeout reports or audits.
Hosted and encrypted in Korea
Personal data is encrypted and stored in AWS's Seoul region, never transferred overseas, with access permissions separated by role.
AI Study Builder

Design with AI, edit the code yourself, and run it directly inside Conveloq

Study code built elsewhere doesn't just run inside Conveloq as-is. The AI Study Builder doesn't just write study code — it also adapts that code to Conveloq's execution structure so it actually runs inside the platform.

  • ✓Describe what you need in plain language to generate study code, then edit any part of it live
  • ✓Even code built elsewhere gets converted and wired into Conveloq's execution structure
  • ✓Get results as a CSV the moment a session finishes — including participation time, reaction time, and drop-outs
AI Study Builder
Build me a Stroop task. 200 stimuli, measure reaction time.
Sure — I've built Stroop task code with congruent/incongruent color-word conditions. Reaction time and accuracy are recorded automatically.
function onTrial(stim) {
  recordRT(stim.onset);
  return nextTrial();
}
✓ Connected to Conveloq's execution structure

We'll handle the hassle of checking everything.
All you have to do is join.

We'll take care of the paperwork.
All you have to do is design the study.

My participation history

From application to reward, all in one view on My Page

See your progress study by study, so you never have to hunt for your application status or when your reward is coming.

  • ✓Track application, confirmed, and completed status in real time
  • ✓Your payout status updates the moment you finish
  • ✓Check payout history and related documents right on My Page
My participation history
All ▾
Online decision-making studyPaid
Working memory & attention taskConfirmed
Consumer privacy surveyUnder review
Negotiation game studyPaid
Document Center

Pick one study and every document you need is right there

From IRB review to grant settlement, see issuance status study by study so you never have to hunt for what to send your admin staff.

  • ✓Download the recruitment notice and study info sheet instantly, identical to your reviewed text
  • ✓Participant rosters are provided only as a pseudonymous-ID CSV — no real names included
  • ✓One settlement statement cuts down the back-and-forth with your grant settlement office
Document Center
Risk Preference Study ▾
Recruitment noticeAvailable
Study info & consent formAvailable
IRB approval documentUpload required
Per-study settlement statementAvailable
What participants worry about

Ever felt uneasy about any of this, joining studies elsewhere?

"

I always had to dig for study postings on community boards, buried between unrelated posts — it was hard to actually find the ones I needed.

Undergraduate participant
"

There was no way to tell if a study was actually approved, so I always felt uneasy before handing over my personal information.

Experienced study participant
"

I'd apply and then have no idea whether spots were still open or when it would run — I just ended up waiting blindly, a lot.

Graduate student participant
What labs struggle with

Running a single study — does any of this sound familiar?

"

A month went by just formatting IRB review documents, before the study had even started. One wrong item and it gets rejected — back to square one.

Psychology graduate researcher
"

After posting the recruitment notice everywhere, the real work was staying up all night manually organizing applicant info in Excel.

Behavioral economics lab assistant
"

The study was done, but I lost count of how many times I went back and forth with the grants office redoing settlement evidence. The paperwork took longer than the results.

Grants office research funding officer
Pre-register

Starting soon

Studies you can join right now

Recruiting now

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FAQ

FAQ

I'm on a D-2 visa (exchange student) — will participating cause problems at immigration?
No. Compensation for study participation is classified as "other income," not wages from employment, so it is unrelated to the activity-outside-status-of-stay (work) restrictions that apply to international/exchange students.
Can I join a study that doesn't have IRB approval?
Yes — research exempt from review under the Bioethics Act is posted only after the institutional review board confirms the exemption. You can always check the approval or exemption status on the study's detail page.
Does every study go through IRB review?
No. Only studies that qualify as human subjects research under the Bioethics Act need IRB approval or a confirmed exemption. General surveys that don't qualify can still be registered, and in that case the detail page shows "IRB not applicable."
See more questions
Document Center
Issue PDF/CSV/Excel documents for the selected research to submit to your IRB, industry-academic cooperation office, or grant settlement staff.

Closing soon — studies you're eligible for

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