Data Management

Meet Madison B., Starting as an intern, she now leads data reviews, investigates anomalies, and supports trials from start to finish.

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

Discover what an effective DMC charter should look like and what contents are required with PharPoint DMC coordinator Victoria.

Principal Data Manager Shantyana R. gives an inside look at her job responsibilities and shares why she believes PharPoint is not your average CRO.

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

PharPoint Lead Data Manager Alyssa L. shares more about her role, her career growth, and what she enjoys about working at PharPoint.

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

What makes database design “smart,” and when should a sponsor start thinking about data collection and analysis? PharPoint programmer Michelle M. explains.

How do you perform non-eCRF data (ECG, Labs, PK) reconciliation in EDC platforms like Medrio? A PharPoint clinical trial expert answers as part of our #askaclinicaltrialexpert blog series.

For our upcoming study, we know we want to use EDC—but there are so many options. How should we choose an EDC provider?