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We are the global biostatistics team dedicated to late phase research working on (but not limited to) peri and post approval research post authorization safety studies observational and non interventional studies patient reported outcomes as well as analyses for abstracts papers and manuscripts.
As a Sr Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design case report form development analysis planning and scheduling analysis and interpretation of data and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.
You will have strong demonstrable experience in:
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Remote Work :
No
Full Time