Position Summary :

To achieve our goals for continued growth, the new position of Senior Statistical Programmer was created in the Biostatistics team. This person will:
Design, develop, evaluate, validate and modify computer programs using SAS to analyze and evaluate clinical data
Produce and deliver standard datasets, program edit checks and produce quality tables, figures and listings in a timely fashion and high quality
Posess thorough knowledge of CDISC theory and implementation guidelines, able to create and validate CDISC standard datasets
Provide expertise in the design and development of clinical trials, protocols, case report forms and clinical databases
Work closely with clinical operations, data management and statisticians on various clinical projects so that data analysis can be performed in a timely fashion
Liaise with vendors as needed to facilitate electronic data transfers

Education And Experience Requirements:

Good project management skills, CRO oversight skills, professional attitude, self-improvement mentality with positive attitude
Good written and oral presentation skills and ability to communicate effectively to other programmers and non-technical colleagues
Ability to think creatively and independently, and to form sound opinions and make sensible decisions in a dynamic environment
Extensive experience working with data management on data checking to ensure locked database in pristine quality
Minimum Bachelor's degree or equivalent level of experience
Experience 5+ years in a pharmaceutical/biotech, CRO setting
R programming experience, a plus
Strong knowledge and understanding of GCP/ICH Guidelines for conducting clinical trials
Strong interpersonal, organizational, and multi-tasking skills
Excellent attention to detail and problem-solving skills
Windows applications: Word, Excel, Powerpoint, etc.