ClinTrust Research exists because clinical trials succeed or fail at the site level — and we built our entire operating model around getting that part right.
ClinTrust is structured around direct relationships with investigator sites and hospital networks across India — built to identify and qualify the right sites for a protocol, including special and hard-to-reach patient populations, rather than relying on generic site lists. Our recruitment strategy is designed around feasibility first: we assess realistic enrollment potential before committing a sponsor's timeline to a site.
This means every site we bring forward has been evaluated against the protocol's actual requirements — infrastructure, investigator availability, and patient population — not just availability on paper.
Every process at ClinTrust — from study start-up through close-out — is built around sponsor visibility. That means structured project tracking, clear financial reporting on investigator payments, and a single point of contact who is accountable for outcomes, not just updates.
We don't believe transparency should be something a sponsor has to ask for. It's built into how we run every study from day one.
The ClinTrust team brings direct experience from CRO and hospital research department environments — not external consultants learning the space, but people who have worked the operational side of clinical trials before building a company around doing it better.
ClinTrust Research was founded by Shivangi Pandey with a vision to strengthen clinical research through operational excellence, quality-driven processes, and trusted partnerships.
Recognizing the growing need for reliable site management support in India's evolving clinical research landscape, she established ClinTrust Research to bridge the gap between sponsors, CROs, investigators, and research sites. Her focus is on building an organization that delivers efficient study execution, regulatory compliance, transparent communication, and patient-centered research practices.
Under her leadership, ClinTrust Research is committed to supporting high-quality clinical trials and contributing to the advancement of healthcare through ethical and innovative research operations.
Every member of the ClinTrust operations team is GCP-trained under ICH E6(R3) standards before working on a live study. We built the company around the belief that sponsor trust is earned through process discipline — not promised through marketing.
Tell us about your protocol and we'll respond with a preliminary feasibility assessment within 24 hours.
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