SAS Programmer II

Job Description:

SAS Programmer II

Working under the direction of the Biostatistician, senior-level SAS Programmer and/or Manager, the SAS Programmer II aids programming activities for various purposes including CSRs, DSMBs, interim analyses, manuscripts, etc. Mainly supports statistical programming of statistical analysis plan (SAP)-planned tables, data listings, and graphs for CSRs, as well as integrated summaries of safety and efficacy, ad hoc analyses and electronic submission deliverables, such as datasets, data documentation, programs, programming table of contents, and patient profiles.

In addition, the SAS Programmer II supports migration activities in the creation of Standard Data Tabulation Model (SDTM) and production of the Analysis Data Model (ADaM).

What we do

For more than 27 years, Veristat has built a reputation as global experts in clinical development.

• 760+ Rare Disease Clinical Trials supported
• 160+ Marketing Applications supported
• In 2022 we supported 8 marketing application that received regulatory approval
• Learn more about our core values here!

What we offer

• The estimated hiring range for this role is $72,000 - $121,000 plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

• Benefits vary by location and may include:
  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for

• Bachelor’s Degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 4 years of SAS programming experience with clinical trial data OR a Master’s Degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 3 years of SAS programming experience with clinical trial data.
• Good working knowledge of CDISC SDTM Implementation Guidelines.
• Good working knowledge of CDISC ADaM Implementation Guidelines.
• General knowledge of regulatory requirements and drug development process.
• Excellent organizational skills and good verbal and written communication skills.
• Ability to work independently as well as collaborate with teams is required.
• Strong communication skill set with peers and business partners.
• Strong data analysis skills.
• Leadership skills to lead project team to deliver high quality deliverables on time.
• Must be fluent in English (written and verbal).

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

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