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Biostatistics, Clinical Programming and Consulting Services

PAREXEL provides high quality deliverables and exceptional service within impressive timelines on every biostatistical project we manage. Whether you require our services as an integral part of a full clinical development program or a standalone consulting service, our Biostatisticians and Clinical Programmers can quickly step in to make a significant contribution to your product development needs.

Our extensive experience in conducting clinical trials from study design through regulatory authority submission enables our Biostatisticians to understand the specifications of your study and respond to your needs. A crucial component of every project is our quality control processes, which include senior-level review throughout each stage of the project or program.

Many companies may offer statistical analysis and reporting. However, you may have specialized needs that go beyond this. PAREXEL’s extensive experience and global resources as a top biopharmaceutical services provider make us the logical choice for Biostatistical and Clinical Programming consulting. Our Biostatisticians are experienced, motivated, and focused on your needs. We offer knowledgeable advice ranging from individual trial design to complete product development programs.

Consulting Services

  • Advice on study design     
  • DSMBs and DMCs    
  • Expert panels   
  • Meeting with regulators   
  • Review of marketing materials
  • Auditing statistical analysis plans   
  • Meta analysis   
  • Publication support   
  • Conference presentations   
  • Post-submission support for ad hoc regulatory authority questions
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About PAREXEL clinical research

Phase I - IV clinical trials management and biostatistics, data management and clinical pharmacology, as well as related medical advisory and investigator site services.