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Form of workJob Description
- Assist in the review and input into project requirement including but not limited to SAP, CRF, and programming specification.
- Develop SAS programs for SDTM, ADaM, e-submission, client-defined analysis datasets, Tables, Listings and Graphs of medium complexity in support of the Statistical Analysis Plan.
- Perform quality control of low-medium complexity within a single project.
- Develop proficiency in technical/programming skills.
- Maintain documentation as appropriate.
MINIMUM REQUIREMENTS:
- M.S. in biostatistics or statistics.
- 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.
CITIZENSHIP
- US citizens and permanent residence preferred, and the company will fully sponsor green card application if needed.
About R&G US:
R&G US/AMIT is a leading Contract Research Organization (CRO) providing full services for clinical trial and entire drug life cycle. Founded in February 2019, 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/AMIT 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/AMIT had extensive experience to support submissions to FDA, EMA, PMDA and NMPA. R&G US/AMIT'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. See more information at rgpharmaus.com.
