Biostatistician/SAS Programmer

🔥 12 hours ago

🇺🇸 United States – Remote

💵 $99k - $129k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 0%

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iRhythm Technologies, Inc.

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2006

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

iRhythm Technologies, Inc. is a medical technology company that specializes in digital healthcare solutions for the management of cardiac arrhythmias. The company is best known for its ZioSuite, a comprehensive platform designed to deliver a streamlined solution for assessing heart health through advanced analytics and patient-centered data collection. iRhythm focuses on improving patient outcomes and optimizing the efficiency of healthcare providers through innovative technology in the cardiac monitoring space.

📋 Description

• Design and analyze clinical trials and observational studies with cross-functional teams • Develop and validate SAS programs for data manipulation, statistical analysis, and report generation • Create and review statistical analysis plans, study protocols, and data specifications • Perform quality control checks on datasets, tables, listings, and figures • Conduct statistical analyses using SAS and interpret results for study, quality, production, and FDA-related objectives • Provide statistical consultation and programming support to Clinical Research, Quality, Production, and other cross-functional teams • Support FDA remediation, regulatory submissions, agency responses, and associated documentation • Present statistical findings and explain analytical methods to internal and external stakeholders • Maintain current statistical methodologies, SAS programming techniques, and best practices for data quality and reproducibility

🎯 Requirements

• Master’s or PhD in Biostatistics, Statistics, or a related field • At least 3 years of biostatistics or statistics work experience • Strong proficiency in SAS programming, including Base, Macro, SQL, and statistical procedures • Experience with clinical trial data and regulatory submissions, including CDISC SDTM/ADaM standards • Knowledge of regression, survival analysis, and mixed models • Familiarity with R or STATA is a plus • Excellent problem-solving, communication, and teamwork skills • Ability to manage multiple projects and meet tight deadlines with high attention to detail

🏖️ Benefits

• Fully remote work arrangement • Reasonable accommodations for qualified individuals with disabilities in job application procedures