Getinge · 18 hours ago
Sr. Clinical Research Statistician
North Waltham, MA, US
Full-time
Hybrid
Mid, Senior Level
$120K/yr - $135K/yr
4+ years expGetinge is dedicated to making life-saving technology accessible for more people. As a Senior Clinical Research Statistician, you will design, validate, analyze, and interpret clinical data to support product development and business objectives, while collaborating with clinical affairs staff and investigators.
BiotechnologyHealth CareLife ScienceMedicalMedical Device
Responsibilities
Use advanced statistical methods to validate and analyze data
Write efficient code for processing data utilizing R statistical software
Create processes for validating quality and accuracy of data
Perform statistical programming and data analysis, as well as database cleaning, verification and validation, and quality review of statistical analyses
Manage resources, timelines and priorities for assigned projects
Work with clinical affairs staff and clinical investigators to determine appropriate study and protocol design
Provide statistical expertise to clinical affairs staff to ensure that the CRFs and database meet the study design needs
Responsible for statistical analysis plans (SAP) and development of tables/listings/figures for statistical reports
Prepare statistical methods and results sections for presentations, reports, and peer-reviewed manuscripts
Participate in preparing and writing statistical content for 501k, Clinical Study Reports (CSRs) and other FDA required reports
May be involved in analyses of ‘big data’ for market assessments, as well as from public sources (such as UNOS)
Organized, self-starter, critical thinker; ability to work in a fast-paced environment with a 'roll up your sleeves' attitude
Ability to work independently and as part of a team
Excellent oral and written communication, and interpersonal skills necessary to interact with a wide range of individuals and cross-functional stakeholders
Qualification
Required
At least 4+ years (MS) or 6+ years (BS) of statistical work experience in a biomedical life science or medical device company, including programming using SAS or R statistical software
Comprehensive knowledge of statistical methods
Prior healthcare or medical device industry experience
Proficiency in R programming skills in a clinical data environment with excellent analytical skills
Knowledge of other programming languages such as SAS, Python etc. is a plus
Prior experience working with research and/or healthcare data
Bachelor's degree in biostatistics, statistics, epidemiology or similar quantitative field of study, required
Proficient in Microsoft Office Suite
Preferred
Master's degree or higher in biostatistics, mathematics or related quantitative field of study preferred
Transplant surgery /medical knowledge is a plus
Experience or knowledge of FDA regulations or submissions is a plus
Benefits
Health, Dental, and Vision insurance benefits
401k plan with company match
Paid Time Off
Wellness initiative & Health Assistance Resources
Life Insurance
Short and Long Term Disability Benefits
Health and Dependent Care Flexible Spending Accounts
Commuter Benefits
Parental and Caregiver Leave
Tuition Reimbursement
Company
Getinge
Getinge identifies customer issues and promotes clinical and economic benefits and follow and support the customer decision process.
10001+ employees
H1B Sponsorship
Getinge has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (3)
2023 (2)
2022 (2)
2021 (2)
2020 (5)
Funding
Current Stage
Public CompanyTotal Funding
$539.31M2017-10-19Post Ipo Equity· $539.31M
2002-06-28IPO
Leadership Team
C
Christoffer Å.
Chief Information Security Officer
Joanna Engelke
EVP Quality Compliance, Regulatory, Medical
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