Job Purpose
Supports project teams through contributions to product development strategies and the design, planning,
execution, analysis, and reporting of clinical studies, with a view toward establishing the conditions essential for
determining safety, efficacy, and marketability.
Major Accountabilities

? Complete understanding and wide application of technical principles, theories, and concepts in the
statistical field.
? Independent operational and technical leadership of multiple protocols in one or more therapeutic areas.
? Under close supervision, may lead efforts related to project‐level activities, to include analyses and inputs
into regulatory filings for all phases of development.
? Ensure and manage quality, timeliness, and efficiency for all support and deliverables for designated tasks.
? Liaise with and provide needed guidance to statistical programmers assigned in support of trial or project
deliverables.
? Establish and maintain working relationships with relevant team functional representation.
Background

Education : ? Doctoral degree in statistics or biostatistics. Master’s degree
with sufficient relevant experience.
Languages: ? Fluent English essential (oral and written)
Experience: ? 0‐3 years with Doctoral degree or at least 5 years with Master’s
degree in the pharmaceutical industry or equivalent.
? Excellent knowledge in statistics and clinical trial methodology.
? Sound knowledge of product clinical development and relevance
to study design.
? Limited or no Health Authority experience.
? Excellent written and oral communication.