Fundación Parque Científico de Madrid seeks a skilled individual to own the statistical strategy behind clinical evidence. The role involves supporting clinical trials and regulatory interactions, designing efficient studies, and optimizing trial efficiency while preserving statistical significance. Candidates should have a MSc/PhD in Biostatistics or related fields, with at least 3 years of relevant experience in applying statistics in clinical contexts. Fluency in R or Python is necessary, alongside strong regulatory submission experience.
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