Job Description
Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Key Responsibilities
* Provide input on study design and analysis plans.
* Develop, validate, maintain, and document analysis programs and other study documents.
* Support the interpretation of results and review publications.
* Review the study concept, protocol design, analysis plans and other study-related documents.
Requirements
* At least 5 years of experience in SAS programming.
* 2+ years experience in Real World Evidence, Epidemiology, or Health Outcomes environment.
* Strong background working with large health care databases such as CPRD or Merative MarketScan.
* Knowledge of R (preferable).
* Good study design and epidemiological and statistical analysis experience.