Broad Biostatistics Clinical Research Acumen

CRO Biostatistics Services

High-quality data analysis is a critical component of all clinical trials. Typically, it is thought by sponsors to occur at the end of a study when the CRO starts reporting results to sponsors and investors. However, Biostatistics can and should also function as an aspect that has value at the outset of the study and at multiple points throughout the clinical development process.

Experience matters. Synteract was founded as a Biostatistics CRO and has more than 4 decades of experience in this area. This longstanding Biostats expertise is offered to our clients in 3 different options: 

  • As part of a full service clinical research project
  • As an FSP solution
  • As a consulting service from our expert PhDs to develop strategies to improve your processes and oversight
  • As a standalone project for those clients who are handling other aspects of trials in-house

As your Biostatistics CRO, our biostatisticians determine the best methods for collecting, analyzing and presenting your data, all in compliance with regulatory guidelines. Our long-tenured team provides creative thinking and analysis optimized for your unique study designs.

You may choose any or all these processes as part of your full-service, consulting, FSP or standalone Biostatistics options:

  • Overall strategy
  • Regulatory strategy for Biostatistics
  • Adaptive design and group sequential strategies
  • Innovative analyses and how to implement - e.g., Lag-time analysis
  • Integration of CDISC into entire study
  • Timeline planning: requirements for each step prior to submission
  • Safety monitoring
  • Consulting on ISS/ISE

Synteract's biostatistics CRO services, offer innovative thinking and analysis that will improve your clinical study design and output with responsiveness that is unmatched in the industry.

Contact Us today to learn how Synteract can provide the best statistical services for your next trial.

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