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Senior Statistical Analyst I (On-Site)

5+ years
$75,300 – $150,700
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Statistical Analyst I (On-site)

Locations: Maple Grove, MN or Santa Clara, CA, USA
Category: Medical and Clinical Affairs


Role Summary

The Senior Statistical Analyst I independently supports biometrics and clinical data analysis for Abbott Medical Devices. The role involves reviewing study protocols, statistical analysis plans, CRFs, and edit check specifications; programming, quality checking, and documenting datasets; and providing statistical expertise to cross-functional teams. May lead a small programming team (1-3 analysts) on assigned projects.


Key Responsibilities

Statistical Programming & Analysis

  • Develop, validate, and maintain complex SAS programs for generating analysis datasets, tables, listings, and figures (TLFs).

  • Conduct quality checks of datasets against source data and validate statistical outputs.

  • Summarize statistical methodologies and interpret results for internal and external stakeholders.

  • Support regulatory submissions, DMC/CEC meetings, IRB packages, and scientific publications with statistical deliverables.

  • Perform ad hoc programming and complex data checks for data management needs.

Collaboration & Project Support

  • Collaborate with clinical, regulatory, and data management teams to define data checking requirements and resolve discrepancies.

  • Partner with cross-functional teams to develop ADS specifications and mock shells.

  • Lead or mentor junior programmers, providing technical guidance and troubleshooting support.

  • Communicate effectively with study teams and escalate critical issues to management as needed.

Quality & Compliance

  • Ensure compliance with Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory standards.

  • Maintain detailed documentation of datasets, programs, and specifications.

  • Set up programming environments, manage study folders, and create or modify project-specific macros.


Qualifications

Required

  • M.S. degree in Statistics, Biostatistics, or related field with 3+ years of experience in statistical or SAS programming
    OR

  • Bachelor’s degree with 5+ years of experience

  • Extensive experience in clinical trial data analysis and SAS programming

Preferred

  • Advanced degree in Statistics, Biostatistics, or related field

  • 2–5+ years’ experience in medical device or pharmaceutical clinical research

  • Experience with highly regulated clinical studies

  • Ability to manage multiple projects under tight timelines

  • Strong verbal and written communication, organizational skills, attention to detail, and team leadership skills


Compensation

  • Base pay range: $75,300 – $150,700 (may vary by location)


Core Competencies

  • SAS programming & statistical analysis

  • Clinical trial data management & validation

  • Documentation & quality assurance

  • Cross-functional collaboration & leadership

  • Problem-solving & project management