• Lead the development, assessment and introduction of new statistical technology and methodology

• Conduct or supervise advanced statistical analyses to address complex design problems across therapy areas.

• Provide statistical sciences training to employees from different disciplines on advanced statistical concepts.

• Communicate complex issues in nontechnical language by using visuals, simulations and other illustrative techniques.

• Lead cross-functional or multi-disciplinary groups and use technical expertise to pro-actively influence business decisions.

• Stay up to date with ongoing developments in statistical methods applications in the pharmaceutical industry.

• Review and approve abstracts, posters, presentations, and manuscripts for publication and ensure accuracy of all biostatistical aspects of such documents.

• 5+ years in biostatistics within the biotechnology and/or pharmaceutical industry (including CROs) with a proven successful track record in pharmaceutical development and statistical methodology.

• Sound knowledge of the ICH guidelines. Understanding of the regulatory requirements from main health authorities (eg, EMA, FDA and PMDA), and of the submission process in each.

• Strong experience with advanced statistical methodologies, in particular Bayesian approaches

• Good knowledge of SAS and/or R programming.

• Excellent knowledge in visualization and simulation techniques

• Ability to travel both domestically and internationally as business necessitates.