The Programmer is responsible for the development, quality control and documentation of statistical

(SAS) programs in support of department projects

Responsible for the development, quality control and documentation of statistical (SAS) programs in support of department projects.

1. Assist in the planning and execution of SAS programming activities for a single project.

2. Assist in the review and input into project requirements.

3. Develop SAS programs in support of clinical trial activities.

4. Perform quality control in support of clinical trial activities.

5. Maintain documentation as appropriate.

SCOPE OF RESPONSIBILITY:

1. Deliver individual programming deliverables of medium to high complexity within a single project.

2. Demonstrate full proficiency in technical/programming skills.

3. Contribute broad knowledge of clinical trial activities.

• 2-3 years as a clinical SAS Programmer with experience in programming and analyzing scientific data, preferably in a pharmaceutical/clinical trial environment.

• Bachelor’s degree and/or equivalent in computer science, mathematics or other scientific field (or equivalent theoretical/technical depth).