Sr. SAS Programmer Job in North Wales 19454, Pennsylvania Us
Role Responsibility
· To design and develop standard software and data structures.
· To develop and execute statistical programs designed to analyze clinical trial information.
· To participate in the development and maintenance of SOPs, including software validation, documentation, study archiving and others as needed.
· To participate in the review of Case Report Forms (design phase), Statistical Analysis Plans, QC Specifications and Database Structures.
· Implement statistical analyses. Develop and execute statistical analyses of clinical trial data under the general guidance of a biostatistician. Design and develop computer programs that produce tables, figures, listings and derived datasets that summarize results of clinical trials.
· Design and implement analysis file structures.
· Review software written by programmer analysts in the department for accuracy and efficiency.
· Monitor procedures for software validation.
· Provide specifications for Programmer Analyst II in the development of standard software and data structures.
Experience Qualification
· Bachelor's degree in scientific discipline with at least five years full-time SAS programming experience in the pharmaceutical, biotechnology or device industries.
· Demonstrated leadership skills as well as ability to work independently and on a team.
· Understanding of data structures, standard software and their implementation.
· Knowledge of the drug development process (Phase I through IV) and general regulatory requirements.
· Good verbal and written communication skills.
