Biostatistical Programmer II

R&G US is a leading Contract Research Organization (CRO) providing full services for clinical trial and entire drug life cycle. As a Biostatistical Programmer II, you will be responsible for developing SAS programs for SDTM, ADaM, e-submission, and client-defined analysis datasets. You will also perform quality control of low-medium complexity within a single project and maintain documentation as appropriate.

• Assist in the review and input into project requirements, including SAP, CRF, and programming specifications.
• Develop SAS programs for statistical analysis and data management.
• Perform quality control of low-medium complexity within a single project.
• Maintain documentation as appropriate.

• M.S. in biostatistics, statistics, data science, public health, computer science, or mathematics.
• Excellent oral and written communication skills in English.
• At least one year SAS programming experience, preferably in a pharmaceutical/clinical trial environment.
• Demonstrate advance SAS skills, macro programming, and SAS/STAT.

R&G US is a fully owned subsidiary of R&G PharmaStudies group company. Led by former FDA experts and industry experts, R&G US can provide 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. R&G US had extensive experience to support submissions to FDA, EMA, PMDA, and NMPA. R&G US's goal is to provide the best service to the clients and work as one team to lower costs, shorten development time, and increase the success probability of products.