Clinical SAS Programmer - Pharma

Looking For clinical SAS programmers for a leading pharma company

Basic qualifications:

- Bachelor's Degree in engineering, Biotechnology, Computer Applications or related disciplines.

- More than 4 years' experience in SAS programming (including SQL and SAS macro language)

- Recognized expertise in SAS programming and SAS macro code development.

- Effective written and verbal communication skills

- Excellent influencing skills, which are applied effectively at all levels of an organization and across multiple functions

- Strong time management skills; able to effectively organize and manage a variety of tasks across different projects

Preferred qualifications:

- Good understanding of other SAS modules (e.g. SAS/GRAPH, SAS Output Delivery System)

- Knowledge of non-SAS programming packages/languages (e.g. Spotfire, S-Plus, R)

- A solid level of understanding of clinical trials, pharmaceutical regulatory and publishing processes (e.g. 21 CFR Part 11)

- Demonstrated knowledge of and experience in the application of CDISC data standards, primarily the creation and use of ADaM datasets.

- Ability to manage conflicting demands and priorities.

- Demonstrated ability to manage the outsourcing or externalization of statistical programming work in the clinical trials setting (e.g., working with CROs, academic institutions)

- Ability to develop creative solutions to applied problems.

- Ability to learn and apply advanced programming skills independently