Job Description
We are seeking a highly skilled RWE SAS Programmer to join our team on a contract basis. This role can be fully remote and is initially for 12 months.
* Support statistical programming activities in Real World Evidence.
* Contribute to study design and analysis plans as needed.
* Develop, validate, maintain, and document analysis programs and other study documents.
* Provide input on interpretation of results and review publications.
* Review study concept, protocol design, analysis plans, and other study-related documents.
Your Background
* 5+ years of experience in SAS programming.
* 2+ years of experience in Real World Evidence, Epidemiology, or Health Outcomes environment.
* 2+ years of experience with large healthcare databases such as CPRD or Merative MarketScan.
* Familiarity with R (desirable).
* Strong study design and epidemiological and statistical analysis skills, including understanding of drug development, observational and epidemiological endpoints, and assessments.
About Our Client
We are a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Location
This role can be fully remote.