Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Biostatistician office based in Poland. Job Overview 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 cleanup to ensure the key study variables are suitable for analysis; Communicate statistical results to medical writing personnel to ensure accurate interpretation. Key Requirements Ph.D. degree in Biostatistics / Statistics with strong experience in SAS Programming or equivalent; 1-2 years of experience in a pharmaceutical or CRO setting preferred. Fluency in both English & Polish Good knowledge of the Pack Office Excellent communication skills
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