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Role Summary
Associate Statistical Project Leader
Responsibilities
Provide high quality input into the design of the clinical study, the setup and conduct of the study
Accountable for all statistical deliverables related to the study
Oversee execution of the statistical analyses according to the statistical analysis plan: perform and/or coordinate with study programmer the production of statistical analyses
Prepare statistical methods & provide statistical insight into interpretation and discussion of results sections for the clinical study report and/or publications to ensure the statistical integrity of the content according to internal standards and regulatory guidelines
Propose, prepare and perform exploratory data analyses, ad-hoc analyses as relevant for the study or project objectives
Provide technical guidance to junior staff
Plan and track study activities and timelines
Ensure productive collaborations with other functions in the aligned study team, promoting teamwork, operational efficiency, and innovation
Represent statistics to participate in scientific or technology working groups or cross function initiatives.
Qualifications
PhD in Statistics or related discipline with at least 3 years of pharmaceutical experience in clinical development, including late phase
MS in Statistics or related discipline with at least 5 years of pharmaceutical experience in clinical development, including late phase
Skills
Broad knowledge and good understanding of advanced statistical concepts and techniques; able to do advanced statistical analyses using SAS or R
Demonstrated strong interpersonal and communication skills
Proficient in written and spoken English
Education
PhD or MS in Statistics or related discipline as listed above