

Senior Statistician
β - Featured Role | Apply direct with Data Freelance Hub
This role is for a Senior Statistician focused on statistical modeling in Cardiac Rhythm Management, requiring an advanced degree and 2+ years of clinical trial data analysis experience. It offers a 6-month remote contract with a pay rate of "TBD" in Minnesota.
π - Country
United States
π± - Currency
$ USD
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π° - Day rate
624
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ποΈ - Date discovered
July 24, 2025
π - Project duration
More than 6 months
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ποΈ - Location type
Hybrid
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π - Contract type
Unknown
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π - Security clearance
Unknown
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π - Location detailed
Minnesota, United States
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π§ - Skills detailed
#CRM (Customer Relationship Management) #"ETL (Extract #Transform #Load)" #SAS #Statistics #R
Role description
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100% Remote role Only in MN!
Sr Statistician- statistical modeling- Cardiac Rhythm Management
Location: CST- Minnesota, MN - In person (Can do WFH)
Local, MN - Should be Physically Present- & Ready to visit the site as needed.
Duration: 6 month + ( possibility of extension )
Shift: Standard shift
Hiring Manager Note:
β’ Unit: Cardiac Rhythm Management (CRM), and Cardiac Ablation Solutions (CAS).
β’ working experience as Statistician/Bio β Statistician
β’ Advanced degree β MS 2+yrs statistics analysis with Bonus of With directly experience on with the design and/or analysis of clinical trial data.
β’ Relevant statistics
β’ Analysing data
β’ design and analysis of clinical trial data
Overview:
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 (CRM), and Cardiac Ablation Solutions (CAS).
Our Cardiac Rhythm Management Integrated 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.
Join a diverse team of innovators who bring their worldview, their unique backgrounds, and their individual life experiences to work every day. Itβs no accident β we work hard to cultivate a workforce that reflects our patients and partners. We believe itβs the only way to drive healthcare forward and remain a global leader in medical technology and solutions.
What are the top 3 things you are looking for in a candidateβs experience:
1. Advanced degree with a minimum of 2 years of statistical experience (e.g., statistical modeling, biostatistics)
1. Experience with the design and/or analysis of clinical trial data.
1. Demonstrated proficiency in SAS statistical software. Experience with R statistical software also beneficial but not required.
Education Required: Advanced degree with a minimum of 2 years of statistical experience (e.g., statistical modeling, biostatistics)
β’ Yearsβ Experience Required: Advanced degree with a minimum of 2 years of statistical experience (e.g., statistical modeling, biostatistics)
Responsibilities may include the following and other duties may be assigned. 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 developmentphase 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.
Thank You!