Lead research design and analytical strategies, provide input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts
Use your expertise to advise, provide guidance and to oversee the quality control of statistical deliverables.
Lead the Biostatistical activities on a study and be accountable for the deliverables.
PhD degree in biostatistics, mathematics, statistics, public health or related discipline with experience in statistical analysis of clinical trials data or MS degree in biostatistics, mathematics, statistics, public health or related discipline with years of experience in statistical analysis of clinical trials data.
Experience with general linear models, mixed models, survival analysis, categorical data analysis and non-parametric methods.
Proficiency in SAS statistical programming.
Knowledge of other statistical and data management software packages is a plus.
Strong written and oral communication skills.
Knowledge and experience with CDISC data standards and models.
Strong project management and mentoring/leadership skills.
In-depth knowledge of applicable clinical research regulatory requirements; e.g., Good Clinical Practice (Google Cloud Platform) and International Conference on Harmonization (ICH) guidelines.
Ability to effectively manage multiple tasks and projects.
Ability to clearly describe statistical techniques and interpret results.
THIRD PARTY AGENCIES, SUBCONTRACTORS, AND RECRUITERS NEED NOT APPLY. Applicants received from firms will not be considered. Subcontracting is not available for this position.