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Go to Clinical Trial Site

Go to Regulatory Management

Become an Investigator

Join the Triallogix Investigator Network

We welcome interest from both experienced principal investigators and physicians who are new to clinical research.

Submit your information to be considered for current and future clinical research opportunities with Triallogix.

Have more questions? Reach out!

info@triallogix.io

(657)-232-7628

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Our Trial Management Solutions

At Triallogix, we've helped research sites like yours successfully navigate regulatory compliance for over 500 studies --and counting.

Our Solutions

IRB Submissions & Oversight

By streamlining submissions, minimizing delays, and safeguarding against compliance risks, we can help you activate studies faster, maintain audit readiness, and build trust with sponsors and participants. Our expertise keeps your trials running smoothly, protects your site’s reputation, and positions you as a preferred partner for sponsors, all while saving you time and resources to focus on quality research.

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Our Solutions

Regulatory Document Management

Stay audit-ready at any moment --with us, your site’s regulatory documents will be meticulously organized, compliant, and ready for audits at any time. By ensuring every essential document is accurate, up-to-date, and easily accessible, we help you avoid compliance risks, maintain strong relationships with sponsors, and meet regulatory standards with confidence.

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More Services

Frequently
Asked Questions

Curious about becoming a PI but unsure of what it entails? Here are some of the most common things people want to know before they join our team.

Who can become a Principal Investigator?

Triallogix specializes in completing, submitting, and managing regulatory documents for clinical research sites. We ensure accuracy, compliance, and timely delivery of essential regulatory documentation.

Can an Investigator continue seeing regular patients

Yes — and virtually all of our investigators do. Research visits are scheduled around your existing clinic schedule, not layered on top of it. Practices typically dedicate one to two half-days per week to research visits, run by our staff in your space.

Why work with triallogix instead of conducting research myself?

Building an independent research site means hiring and retaining certified coordinators, purchasing equipment, building regulatory infrastructure, negotiating your own contracts without benchmark data, and getting on sponsor radar with no track record. That's a six-figure investment and 12–18 months before a first enrollment, with real risk of never being selected. We've already built it. You contribute the practice, the patients, and the clinical oversight.

How much time does a PI need to commit?

Most of our investigators spend two to four hours per week on research. You perform the visits that require a physician — eligibility determination, medical assessments, safety review, adverse event evaluation, and signing off on source. Our coordinator handles scheduling, consent administration, data entry, sample processing, monitor visits, and sponsor queries. Time commitment scales with the number of active studies, and you control that number.

What makes a a site successful?

Enrollment. Sponsors track it, and it determines whether you get invited to the next study. Sites fail on recruitment far more often than on data quality, which is why we run recruitment in-house rather than leaving it to your front desk. The second factor is clean, timely data — which is a function of coordinator quality, and our coordinators do this full time.

Can Triallogix work with my existing regulatory systems or templates?

info@triallogix.io

657-216-1255

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Join the Triallogix Investigator Network

Our Trial Management Solutions

IRB Submissions & Oversight

Regulatory Document Management

FrequentlyAsked Questions

Frequently
Asked Questions