For sponsors & CROs

You can't control enrollment speed when you can't control protocol interpretation.

Eighty-seven sites. Eighty-seven slightly different reads of your protocol. TrialPulse makes every site — across every country, through every amendment — operate from the same interpretation. Your medical monitor can't be everywhere. TrialPulse can.

amendment v2.1 · rollout
Detected §5.3 dosing window 7d → 5d
Routed 87 sites · 14 countries
Verified 94% comprehension in 3 days

Industry average to operationalize: 6.4 weeks.

What TrialPulse delivers

Four levers that move your timeline — and your trial budget.

Faster enrollment

Coordinators get protocol-aligned answers in seconds. Borderline cases resolve instantly instead of waiting on a monitor email.

Better site engagement

Your study stays top-of-mind from SIV to last-subject-in — not buried under ten other protocols on a coordinator's desk.

Improved physician awareness

Open cohorts surface to the right physicians by biomarker, at the point of care — turning passive sites into active referrers.

Real-time trial visibility

One live operating picture across the portfolio: decision time, comprehension, and confusion hotspots before they become deviations.

The full picture

Everything TrialPulse delivers to CROs & sponsors.

Beyond timelines and budget — the operational wins your sites feel at every decision point.

Eliminate Protocol Interpretation Variability

Every site—from Boston to Munich to Tokyo—interprets eligibility criteria identically. No more 'slightly different' enrollments. No more data inconsistency.

Prevent Deviations Before They Happen

Real-time AI guidance catches eligibility errors at the point of decision—not months later during monitoring. Reduce preventable deviations by up to 40%.

Accelerate Enrollment Timelines

Sites don't hesitate. Coordinators get protocol-aligned answers in 5 seconds. Borderline cases get resolved instantly. Enrollment velocity increases.

Reduce Screen Failure Waste

Sites stop over-excluding patients 'to be safe.' AI clarifies edge cases, reducing unnecessary screen failures and maximizing site budget efficiency.

Improve Diversity & Inclusion

Standardized eligibility interpretation reduces unconscious bias in screening. Sites confidently enroll underrepresented populations when criteria are crystal clear.

Lower Monitoring Burden

Fewer deviations = fewer queries = fewer corrective actions. CRAs spend less time on reactive problem-solving and more time supporting proactive site performance.

Keep Studies Top-of-Mind

Continuous engagement through AI-powered protocol updates, training refreshers, and eligibility reminders. Your study doesn't get lost in the stack.

Onboard New Staff Instantly

SIV materials and training videos stay accessible 24/7. New coordinators joining mid-study onboard in hours, not weeks—without relying on colleagues' fading memory.

TrialPulse Oncology Intelligence — searching open trial cohorts by biomarker, variant, cancer type and line of therapy

Schedule a Demo

Tell us a little about your study and we'll tailor the demo to your protocol.