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Biostatistics and Programming

At the heart of every advancement in clinical research is the ability to turn complex data into actionable insights.

With Seriant’s biostatistics and programming expertise, your data becomes a powerful tool for decision-making, driving your clinical research programs forward with confidence.

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Our Biostatistics and Programming teams bring decades of expertise to help you make informed decisions, from study design to statistical analysis, final reporting and publication.  We offer expert solutions tailored to meet your needs while maintaining the highest standards of scientific integrity. 

Our end-to-end services are available as an integrated component of a full-service contract or as à la carte options, designed to ensure your project progresses smoothly from protocol to publication. We partner with you and provide dedicated support for seamless execution and timely deliveries.

Since its inception, Seriant has empowered companies and researchers to confidently advance their clinical trials. 

  • Our dedicated team of highly skilled clinical programmers tailor solutions to your needs.
  • We offer CDISC-compliant programming and can support a wide range of clinical trial programming needs.

Our team of biostatisticians collaborate with you to design and analyze studies of any size, optimizing trial outcomes.

  • Sample size and power calculation for robust study results
  • Statistical expertise in protocol development and study methodology
  • Randomization list
  • Support for Data Safety Monitoring Boards, interim analyses, and safety committees
  • Participation in regulatory discussions
  • Statistical writing for clinical study reports, abstracts, and publications

We pride ourselves on delivering high-quality statistical outputs and reports with precision and efficiency. Our team ensures that your project remains compliant while producing precise and reliable reports. We provide: 

  • Statistical analysis plan
  • Derived datasets, including in CDISC format (ADaM, define.xml files, reviewer’s guide)
  • Tables, listings, and figures for interim and final analysis
  • Ad hoc analysis

Equipped with cutting-edge tools and software, including SAS and PASS, we’re able to deliver high quality statistical analysis. We are committed to producing robust results and providing support throughout your study lifecycle.

  • State-of-the-art statistical software tools for accurate results and efficiency
  • Dedicated support to ensure timely delivery and client satisfaction
  • Work hand in hand with Project Management so that all statistical deliverables are well planned and executed on time
  • Support for key milestones (i.e. interim analyses, database lock, unblinding and more)
  • Provide ongoing statistical consulting and expert guidance throughout the project lifecycle
  • Support the clinical and medical data review teams ensuring data accuracy, clinical relevance, and informed decision-making
  • Offer full service and standalone statistical support & expert consulting to meet your needs

Interested in this service?
Let’s work together!

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