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Veristat

Senior SAS Programmer

Job Posted 14 Days Ago Reposted 14 Days Ago
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In-Office
Chennai, Tamil Nadu
Senior level
In-Office
Chennai, Tamil Nadu
Senior level
The Senior SAS Programmer leads programming for CSRs and ad hoc analyses, supporting the creation of tables, data listings, and graphs based on the statistical analysis plan. Responsible for SDTM migration and ADaM production, while also monitoring milestones and leading a team to ensure high-quality deliverables are met on time.
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Job Description:

SENIOR SAS PROGRAMMER

The Senior SAS programmer leads the 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 Senior SAS Programmer supports migration activities in the creation of Standard Data Tabulation Model (SDTM) and production of the Analysis Data Model (ADaM).  The Senior SAS Programmer is also responsible for monitoring and meeting assigned program milestones and will lead a team of programmers to accomplish tasks.

VERISTAT INFO

For more than 30 years, Veristat has built a reputation as global experts in clinical development, registration, and post-marketing solutions. We have done so by hiring talented people whose core values are aligned with ours and who share a common passion for our mission driven work.

We do things differently than other CROs and would love to have you join our Veristat team!

Experience & Minimum Requirements

  • Bachelor’s Degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 8 years of SAS programming experience with clinical trial data OR Master’s Degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 6 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.
  • Excellent organizational skills and good verbal and written communication skills.
  • Ability to work independently as well as lead programming teams.
  • Strong communication skill set with peers, business partners, and Sponsors.
  • Strong Analytical mindset.
  • Leadership skills to lead project team to deliver high quality deliverables on time and work directly with the Sponsor to meet the project delivery expectations.
  • 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.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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