Senior Biostatistician

Experience

7+ Years

Education

• Master's degree in Statistics or equivalent
• Ph.D. in Statistics or equivalent & ≥ 4 years of industry related experience

Skills to have

Sr. PS Specifics

The Biostatistician is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. With appropriate experience, biostatisticians can have responsibilities for integrated summaries and / or supporting a particular indication of an asset. These individuals develop collaborative relationships and work effectively with the GBDS (Global Biometric Sciences) Biostatistics Lead, medical monitor, protocol manager, data manager, PK scientist, and other members of the study / indication team. Biostatisticians are individual contributors and report to a GBDS Lead.

The Biostatistician is responsible for strategic and scientific contributions at the indication / protocol / integrated analysis level. These contributions lead to better understanding of the asset being studied, improved development decisions, and an increased likelihood of regulatory and market success. This role has significant stakeholder management responsibility with business partners on their team. The biostatistician III has responsibility for driving selection of optimal study designs, data collection, analytic approaches and rigorous interpretation of trial data. This person may interact with external vendors, key opinion leaders and regulatory agencies.