|The Statistician contractor supports TA Lead Statisticians and Trial Statisticians through contributions to the design, planning, execution, analysis, and reporting of clinical studies. Major position accountabilities include:
Complete understanding and wide application of technical principles, theories, and concepts in the statistical field.
Independent operational and technical support of multiple protocols in one or more therapeutic areas.
Under close supervision, may support 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.
Skills The following skillset is required:
Excellent knowledge in statistics and clinical trial methodology.
Sound knowledge of product clinical development and relevance to study design.
Proficiency in SAS.
Limited or no Health Authority experience.
Excellent written and oral communication.
Excellent organizational skills.
Fluent English essential (oral and written).
0-3 years experience with Doctoral degree or at least 3 years experience with Master's degree in the pharmaceutical industry or equivalent.
Education 0-3 years experience with Doctoral degree or at least 3 years experience with Master's degree.