Clariva Data Solutions is a full-service clinical data solutions provider, bringing enterprise-caliber expertise across Clinical Data Management, Biostatistics, Medical Coding, and Medical Writing to biotech and pharmaceutical companies.

Founder & Principal Consultant
Clariva Data Solutions was founded with a clear mission: to bring enterprise-caliber clinical data management expertise to biotech and pharmaceutical companies that need it most, without the overhead of a CRO.
With over 20 years of hands-on experience across Phase I through Phase IV clinical trials, I've managed data for studies spanning oncology, medical device, vaccines, immunology, and more. I've worked within both sponsor and CRO environments, giving me a unique perspective on what it takes to deliver clean, compliant data on time.
What began as Clinical Data Management has grown into a full-service clinical data team. Today Clariva also delivers Biostatistics and Statistical Programming, Medical Coding (MedDRA and WHODrug), and Medical Writing, so sponsors can engage one capability or the full suite under a single, accountable partner.
Clariva is derived from the Latin word for clarity, because clear data leads to clear decisions, and clear decisions advance better medicine. If you're looking for a trusted partner who can step in, build structure, and deliver, I'd love to connect.
A disciplined, repeatable process that works whether we run the work or oversee a partner doing it.
Learn everything about your trial protocol, EDC platform, CRO relationships, timelines, and where the gaps are. No assumptions.
Review CDM documentation and, when overseeing a CRO, invest time understanding their team, processes, and strengths to build a true working partnership, not just oversight.
A clear, prioritized roadmap: what needs to happen, in what order, by when, and who owns it.
Build, review, oversee, and escalate as needed, all the way through database lock and submission readiness.
Full service or a la carte. Engage the entire team or just one capability. There is no all or nothing. Every department is available for full service, oversight only, or focused support to help complete a specific activity.
Every edit check, every query, every dataset — we apply rigorous attention to detail because in clinical data, precision saves lives.
We uphold the highest standards of data integrity and regulatory compliance, treating your data with the seriousness it demands.
Clear communication, defined processes, and no surprises. You'll always know where your study stands.
Whether you need full-service support or targeted expertise, I'd love to hear about your project.
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