Provide statistical inputs on study projects, especially in the field of statistical methodologies in study design, sample size estimation, statistical modeling, data handling, analysis and reporting
Work with Biostatistics team to develop and validate SAS codes for the analysis of clinical study data, generate output tables, listings and graphs in according with the study protocol and the statistical analysis plan (SAP)
Work with PK/PD scientists to prepare SAP
Generate randomization scheme for clinical studies
Provide technical advice to junior Biostatisticians as well as Statistical Programmers assigned to the program/projects.
Work with PK/Biostatistics team to prepare and review SOPs
Review statistical outputs and clinical study report
Work with Data Management team to provide inputs for the specifications of domains and the creation of CDISC ADaM datasets
Provide statistical consultations to the clients
Job Requirements:
M.Sc in Statistics or Biostatistics, experience with SAS/Base, SAS/Macro, SAS/SQL and SAS/Graph
Strong experience with statistical methods and modeling
At least 3 years of Biostatistician experience in the pharmaceutical industry or in the field of clinical research is required
Proficiency with Microsoft Office
Good interpersonal skills, good communication skills
Attentive to details, good initiative and able to work with changing priorities
