PAREXEL's team of data sciences experts offers available resources from over 650 professionals worldwide, with the capability to work together as one on the same clinical database.
Our experts realize that analysis is a critical function in your clinical trial and will address your needs by providing you with our extensive knowledge of technologies in the following areas:
PAREXEL places a strategic concentration on facilitating project level and program level planning, and eClinical. Our experts have a deep understanding of regulatory expectations and will ensure you are up to date with all regulatory initiatives, helping you to reach your goal of regulatory approval.
A full-service provider, focusing on your goal
Clinical data management experts
With over 650 Data Management professionals, PAREXEL has established one of the largest clinical data management departments in the world over the past 25+ years. We're experienced in both traditional paper and Electronic Data Capture trials, and our CRF design department has a worldwide reputation. PAREXEL maintains a pre-eminent reputation in Biostatistics and Clinical Programming services. PAREXEL Biostatisticians and Clinical Programmers streamline the drug development process by collaborating with Data Management, Regulatory, Project Management, Medical, Clinical, and Medical Writing for the efficient collection, analysis, and reporting of data.
Our team approach to clinical data management
We work closely with our Clinical and Biostatistics departments in order to produce high quality data with a trouble-free database lock.