We are the global biostatistics team dedicated to late phase research, working on (but not limited to) peri and post approval research, post authorization safety studies, observational and non interventional studies, patient reported outcomes as well as analyses for abstracts, papers and manuscripts.

As a Sr Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.

• Designing, developing, validating and documenting SAS programs to generate analysis datasets, generate summary tables, figures and listings.

• Support statisticians in the development and review of Statistical Analysis plans and programming specifications

• Responsible for assisting data management with implementing protocols and CRFs

We are looking for:

• Bachelors or Master's degree in statistics, biostatistics, or related field

• SAS Programming experience – (ideally 5 yrs or more)

• Major experience in the Pharmaceutical/CRO industry