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*Contribute to clinical development of plan preparation;
*Review of study protocol and preparation of statistical methodologies;
*Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports;
*Communicate project requirements for CRF design, database design and database clean-up to ensure the key study variables are suitable for analysis;
*Communicate statistical results to medical writing personnel to ensure accurate interpretation.
·Ph.D. Biostatistics/ Statistics, with strong experience in SAS programming or equivalent.
· Fluent in both French and English
·Previous experience working in a pharmaceutical or CRO setting is desirable.