PhD Researcher in Clinical Trials

4 days ago


London, Greater London, United Kingdom Medpace Full time
About the Role

The ideal candidate will have a Ph.D. degree in Biostatistics, Statistics, or Medical Statistics and experience in SAS programming. Knowledge of advanced statistical methods and the pharmaceutical industry is essential.

Responsibilities include contributing to clinical development plan preparation, reviewing study protocols, and developing detailed Data Analysis Plans. The successful candidate will also communicate project requirements for CRF design, database design, and database clean-up.



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