Strong general knowledge of statistics and quantitative methods with at least 8 years working in clinical development in the pharmaceutical industry.
Knowledge of clinical trial study design, application of appropriate statistical methods, and implementation of simulations (R and SAS).
Strong oral and written communication skills are requirements as a key contact person working possibly CRO partners.
Statistical programming may be required for oversight of deliverables from internal or outsourcing through CRO. Hands on statistical and programming work required. Knowledge of CDISC preferred.
Minimum requirement is MS degree (PhD preferred) in statistics, biostatistics, or a quantitative analysis field.
