SAS Programmer, Real World Evidence

Responsible for performing SAS programming (validating listings, locked datasets, analysis data sets, tables, listings, graphs,...) in accordance with study specifications, applicable guidelines, regulatory requirements and SOPs. 

Responsibilities:

• Responsible for designing, developing, validating and documenting SAS programs to generate data listings for data review, create raw datasets and analysis datasets, analyze data; generate summary tablets, figures and listings,...

• Responsible for assisting statisticians in the development and review of Statistical Analysis plans and programming specifications

• Responsible for assisting data management with implementing protocols and CRFs

• Responsible for assisting data management  in development and programming of edit specifications

• Responsible for integrating data from different sources and formats

• Responsible for providing data transfers to clients as specified

• Participate in the improvement of the Quality Assurance System

• Completing other appropriate duties, as assigned by the manager, which require similar skills in accordance with business needs

Education and Experience:

• Bachelor's Degree preferably in statistics, computer science, or mathematics

• Minimum 2 years of SAS programming experience in a biotechnology, pharmaceutical, CRO or other health care setting

• Strong SAS programming skills and understanding of database structures

• Ability to use structured programming techniques

• Ability and willingness to use and/or modify existing programs and macros

• Understanding of common clinical database terminology and standards

• Knowledge of basic statistical research designs and methodologies in clinical and epidemiological research

• Good knowledge of ICH-GCP guidelines or other relevant guidelines (GEP, GPP...) or industry standard 

• Ability to work effectively and cooperatively with other team members

• Good written and verbal communication skills