Statistical Programmer

Primary Job Function

Responsible for the integrity of the programming/computing solutions for multiple clinical trials (or equivalent) and/or publication activities.

In collaboration with the Biostatistician and Senior Programmer, provide programming support to project-level programming deliverables and other adhoc programming requests.

Roles and Responsibilities

• Ensure understanding and compliance with study and project programming standards. Responsible for development of programming specification.
  
• Create and Validate Safety and Efficacy Analysis Datasets in adherence with CDISC and client specific standards and maintain quality and accuracy.
• Create and Validate Safety and Efficacy Tables, Listings and Figures with high quality and accuracy.
• Create Study specific or general macros and finalize programming specifications/mock-ups.
• Adhere to programming specifications and study specific requirements, including completion and filing of required documentation.
• Plan and organize workload to ensure effective time management and adherence to project specific timelines.
• Proactively plan for and implement effective resource planning, task allocation and tracking of workload in accordance with agreed KPIs and quality standards
• Trouble-shoot and resolve programming issues in a timely and efficient manner.
• Ability to work independently and as part of a team environment.

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• Strong problem solving and organizational skills, attention to detail, verbal and written communications skills

Desired Candidate Profile

• Create and Validate Safety and Efficacy Tables, Listings and Figures with high quality and accuracy.
• Very strong SAS programming skills required in SAS/Base, PROC SQL,SAS/Stat, SAS Macros and SAS/Graph (Base and Advance SAS).
• Good communications and negotiation skills, ability to work well with others globally.