Key support needed to drive your trial
DEPENDABLE EXPERT STATISTICAL PROGRAMMERS SUPPORTING YOUR SUBMISSIONS
Our dedicated teams of statistical programmers provide the support needed to keep your trial at a good pace. We are adept at analyzing clinical trial data to execute on-time and accurate deliverables. Our statistical programmers work to make your Tables, Listings & Figures submission and audit-ready.
Leverage our Flexible and Customized Statistical Analysis Support
Our highly skilled and experienced team of project managers, leads, and senior programmers will successfully guide you through the most complex clinical trials. Our experts are well versed in:
- SAS & R Programming
- SDTM & ADaM Mapping & Generation
- Define.xml Generation
- Tables, Listings, & Figures (TLFs)
- Analysis Dataset Programming
- Ad hoc Analysis Programming
- Statistical Analysis Programming
- QC & Verification Programming
- PK|PD Programming & Analysis
- CSR, ISS/ISE, & Annual Report Support
- Registry, Post Marketing, & Manuscript Support
- SAS Macro Development
Meet the challenges of data requirements in your clinical trials with our flexible global FSP
Learn about our Statistical Programming support for an urgent ISS for a top 20 global pharma
Leverage Our Expertise
Benefit from over 25 years of experience and a drive to constantly be apprised with the latest industry standards has helped us cater to the needs of even the most complex clinical trials.
- We work Smart.
- We work Efficient.
- We work with YOUR needs in mind.
Get in touch
Ready to explore how Navitas Data Sciences can make your clinical programming platform more efficient and flexible?
Please feel free to contact us so we can get started supporting your team of experts.