Biostatistics
High Quality, Efficient, Biostatistical Support
Strong biostatistical support is essential to the design and execution of efficient, high quality clinical trials. Our trained, qualified, and experienced biostatisticians can help take your clinical trial or observational study from concept all the way through final analysis and reporting.
Paired with our proprietary technology, Veridix, our statisticians deliver:
Cleaner data and faster timelines through seamless integration with our eClinical systems
Real-time insights for proactive study oversight
Validated, reproducible, submission-ready analyses
Our Legacy. Our Future.

Emmes Biostatistics Spotlight: How are Emmes’ Statisticians involved throughout a clinical trial?
Biostatistics Experience
We have managed biostatistics for over 1,000 clinical trials, from simple Phase I-II to highly complex, global Phase II-IV trials and registries. Our team has experience with adaptive designs, independent reporting to Data Monitoring Committees (DMCs) and Data and Safety Monitoring Boards (DSMBs), production of CDISC compliant deliverables such as SDTM and ADaM datasets, metadata, and reviewer’s guides and PK/PD analyses.
Our experience across numerous therapeutic areas is complemented by specialist expertise in vaccines, infectious diseases, substance use disorder, neurology/mental health, ophthalmology, oncology, maternal and child health, transplant, allergies, autoimmune disorders and gene/cell therapies.


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