Senior SAS Programmer

Posted 12 Days Ago
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Chennai, Tamil Nadu
Senior level
Other
The Role
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.
Summary Generated by Built In

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 27 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.

Top Skills

SAS
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The Company
Basel
443 Employees
On-site Workplace

What We Do

Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies.

At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. ​

With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases.

We are…Bold. Scientific. Versatile. Veristat.​

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Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at [email protected]. Be vigilant

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