Clinical Statistical Programmer - SAS - Healthcare

- Key contributor responsible for statistical programming of deliverables for assigned studies or project-level activities under guidance of a Trial Programmer.

- Create primary program to generate deliverables in accordance with TFL shells, programming instructions and programming dataset specifications

- Validate deliverables

- Create study, project or global macros

- Contribute to the development and review programming dataset specifications Ensure quality, timely and efficient completion of deliverables

- Good SAS programming skills/develop SAS programs including development and use of macros

- Good working knowledge of statistical concepts

- Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, ICH) and industry standards such as CDISC

- Good understanding to generate/validate/ analysis of datasets, TFLs/statistical analysis from clinical datasets, analysing plans/programming dataset specifications/ TFL shells/ programming instructions.

- BA/BS/MS or equivalent experience in mathematics, statistics, computer science, health sciences or related field will be preferable.

- At least 3 years of relevant programming experience

- Relevant programming experience is in the pharmaceutical or device industry Education