Sr. Statistician (5 month contract // Hybrid in Mounds View, MN):
Top 3 Required Skills:
1. Advanced degree with a minimum of 2 years of statistical experience (e.g., statistical modeling, biostatistics)
2. Experience with the design and/or analysis of clinical trial data.
3. Demonstrated proficiency in SAS statistical software. Experience with R statistical software also beneficial but not required.
Education Required: Advanced degree in Statistics, Biostatistics, or Epidemiology with a focus on Statistics
Years’ of Experience Required: Advanced degree with a minimum of 2 years of statistical experience (e.g., statistical modeling, biostatistics)
Summary:
In this exciting role as a Senior Statistician, you will have primary focus responsibility to support innovative cardiovascular device and ablation device clinical trials and contribute to efforts in the field of advanced analytics and data solutions. The Senior Statistician will support Cardiac Rhythm Management and Cardiac Ablation Solutions. Our Cardiac Rhythm Management Operating Unit offers devices and therapies that treat patients with abnormal heart rhythms and heart failure. Together, we will transform the lives of people with cardiac arrhythmias and heart failure. This role will support the design, analysis, and publication of clinical trial data.
Duties:
• Designs, plans, and executes biostatistical components of plans for research and development projects that establish the conditions essential for determining safety, efficacy, and marketability of pharmaceutical and/or biological products
• Uses sound statistical methodology to conduct studies relating to the life cycle of the product. In development phase projects, prepares the statistical component of protocols which meet project objectives, health authority guidelines, and clinical trial methodology standards
• Develops and/or applies statistical theories, methods, and software.
• Summarizes and interprets data into tabular and graphical formats amenable to principles of statistical inference and is responsible for the statistical component of reports describing studies, outcomes and methods used
• Provides specifications and directions to the clinicians/statistical programmers.
• Supports the regulatory review and approval of the experimental therapies
• May partner in trial design and in establishing standards for clinical conduct, and the collection, management and/or reporting of data
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