Main Responsibilities: Responsible for the implementation and use of programs to effectively analyze and report clinical trial data as the trial programmer. Responsible for the review of trial documentation and providing feedback from statistical programming perspective, as
The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output, including, but not limited to: ADaM datasets, tables, figures, and listings output
Job Description You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead. In this role, you will: