Biostatistics

Get to know PharPoint statistical programmer Maegan F.

Meet Mary H., PharPoint’s Associate Director of Biostatistics, including her career journey and what drives her passion and success.

This brief guide provides timeline benchmarks for Sponsors evaluating biometrics contract research organizations (CROs).

Why engage a biostatistician early in the study design process, and how do you identify the right consultant for your study?

How can an experienced biostatistician provide critical support before and during the regulatory submission process?

Discover key interactions between clinical data management and biostatistics teams for a more efficient clinical trial.

Learn more about what makes working at PharPoint Research unique and get to know biostatistics manager Carson M.

Learn more about the journey clinical trial data takes before ending up on the package insert of a drug you’re taking.

How do our experts produce quality statistical analyses? Proper planning, processes & review are critical.

Learn more about the shifting CRO landscape, as PharPoint’s manager of programming technologies discusses adaptive trial design and outsourcing with EDC provider Medrio.