Accelsiors provides statistical services across a wide range of therapeutic areas and all phases of clinical research. Our biostatisticians play an important role in the design, conduct, analysis, and reporting of randomized controlled trials. They work closely with study team and Sponsor Representatives to achieve the best study design for each protocol. We aim to propose the study design that best answers the research questions, ensuring adequate power and proper randomization.
Our Biostatistician team of well educated, young, dynamic and dedicated people with the support of senior statisticians is offering the following services:
- Protocol review
- Statistical input to the study design
- Sample size determination
- Input and review of CRF/eCRF design
- Generation of randomization codes
- Creation of Statistical Analysis Plan
- Statistical programming
- Design of statistical tables, figures and data listings
- Creation of Statistical Reports and contribution to Clinical Study Report
- SAS programming
Our team actively participate in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies as required.
We are well aware how important the planning in clinical research is. The Statistical Analysis Plan (SAP) early on in the study is vital in our operations. Detailed description how data will be analyzed may support and streamline the data monitoring and data collection methods.
Strong clinical and data management background of employees, excellent cooperation within Biometrics and with other Accelsiors Units (Clinical, Safety and Medical Management, Medical Writing) will ensure quick and precise collection, analysis and reporting of clinical study data.
