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