Principal Statistical Programmer

Responsibilities:

Perform SAS programming activities to meet timelines, budget, and quality in accordance with Company study contracts and SOPs

Effectively work with Biostatisticians and Statistical Programming team to review data specs, generate or QC analysis datasets and generate or QC analysis outputs per requests for internal medical monitoring, CSR and submission needs

Work with data managers to generate ongoing outputs to support data cleaning and to enhance data integrity

Communicate effectively within Biometrics and with cross-functional team members

Work on special projects as needed

Support internal analysis data and reporting deliverables. Ensure timely, targeted, and accurate reporting and outcomes.

Requirements:

Bachelor's Degree in statistics, computer science or another related science field with a minimum of 5 years of SAS programming experience with clinical trial data OR master's degree in statistics, computer science or another related science field with a minimum of 8 years of SAS programming experience with clinical trial data

Good working knowledge of CDISC SDTM and ADaM Implementation Guidelines

General knowledge of regulatory requirements and drug development process

Strong verbal and written communication skills

Ability to work independently as well as part of programming teams

Strong communication skill set with peers and other group partners

Consistently deliver high quality deliverables on time and meet the project delivery expectations