Background information about the job or company

IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...

Responsibilities or duties

As a Senior Statistical Programmer you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas. You will also provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs. You will plan and lead the development of project-related solutions to the full scope of statistical programming tasks.

As a lead programmer on assigned studies, you will write and maintain programming specifications datasets and program TLFs, to maximize programming efficiency with the use of biostatistical tools and assist in training and mentoring new or junior team members

Qualifications or requirements

• Bachelors or Masters’ in Computer Science, Mathematics or equivalent
• 3+ years, statistical programming experience within the Life Science industry
• Experience as project lead, directly engaging clients and coordinating tasks within a programming team
• Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
• Ability to independently lead multiple tasks and projects

• Write and maintain programming specifications datasets and program TLFs
• Maximize programming efficiency with the use of biostatistical tools
• Assist in training and mentoring new or junior team members
• Plan and lead the development of project-related solutions to the full scope of statistical programming tasks
• Provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs

• Base SAS
• SAS/STAT
• SAS Graph
• SAS Macro Language
• Project leadership
• Client engagement
• Task coordination
• Clinical research regulatory knowledge (GCP, ICH)
• Independent task and project leadership

• Bachelors or Masters’ in Computer Science, Mathematics or equivalent
• 3+ years, statistical programming experience within the Life Science industry
• Experience as project lead, directly engaging clients and coordinating tasks within a programming team
• Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
• Ability to independently lead multiple tasks and projects