Job Description

R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical trial and entire drug life cycle. 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. You may find more information at .

If you are interested, please email your CV to: info@rgpharmaus.com.

As a biostatistical/SAS programmer I, you are responsible for the following tasks:

• Develop SAS programs for SDTM, ADaM, Tables, Listings and Graphs of low complexity in support of the Statistical Analysis Plan.
• Support data management by generating data listings.
• Perform quality control of low- complexity tasks.
• Develop proficiency in technical/programming skills.
• Maintain documentation as appropriate.

Minimum Requirements:

• M.S. in biostatistics, statistics, mathematics, computer science or related field. 
• Excellent oral and written communication skills in English.
• Hands on SAS skills in Base and advanced SAS, basic Macro programming and SAS/STAT.

Citizenship:

• US citizens and permanent residence are preferred.

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