Statistical Programming Analyst II

1 week ago


Somerset, United States R&G US Full time
Company Overview:
R&G US Inc. is a Contract Research Organization (CRO) dedicated to supporting pharmaceutical and biotechnology firms in the planning, analysis, and submission processes of clinical trials.

Position Summary:
As a Statistical Programming Analyst II, you will be tasked with a variety of responsibilities that are crucial to the success of our projects. Your role will include:
  • Contributing to the evaluation and input of project requirements, which encompass but are not limited to the Statistical Analysis Plan (SAP), Case Report Forms (CRF), and programming specifications.
  • Creating SAS programs for Standard Data Tabulation Model (SDTM), Analysis Data Model (ADaM), electronic submissions, and client-specific analysis datasets, as well as generating Tables, Listings, and Graphs of moderate complexity in alignment with the Statistical Analysis Plan.
  • Conducting quality control checks of low to medium complexity within individual projects.
  • Enhancing your technical and programming skills to achieve proficiency.
  • Ensuring proper documentation is maintained as necessary.

Minimum Qualifications:
  • Master's degree in Biostatistics, Statistics, Data Science, Public Health, Computer Science, or Mathematics.
  • Strong verbal and written communication skills in English.
  • A minimum of one year of SAS programming experience, ideally within a pharmaceutical or clinical trial context.
  • Proven advanced SAS capabilities, including macro programming and SAS/STAT.

Citizenship Requirements:
  • Preference will be given to US citizens and permanent residents; the company is willing to fully sponsor green card applications if necessary.

About R&G US:

R&G US/AMIT is a prominent Contract Research Organization (CRO) offering comprehensive services for clinical trials and the entire drug development lifecycle. Established in February 2019, R&G US operates as a wholly owned subsidiary of the R&G PharmaStudies group. With leadership from former FDA and industry experts, R&G US/AMIT is equipped to deliver end-to-end services in strategic planning, clinical trial design, statistical analysis, SAS programming, data management, medical writing, medical monitoring, pharmacovigilance, and Data Monitoring Committee services. Our extensive experience includes supporting submissions to regulatory bodies such as the FDA, EMA, PMDA, and NMPA. R&G US/AMIT is committed to providing exceptional service to our clients while working collaboratively to reduce costs, shorten development timelines, and enhance the success rates of products.



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