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Senior Statistical Analyst I (On-Site)

5 years
$75,300.00 – $150,700.00
10 Sept. 9, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ 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

Sr. Statistical Analyst I

Location: On-site, Maple Grove, MN or Santa Clara, CA
Business Unit: Abbott Medical Devices – Biometrics Team


About Working at Abbott

At Abbott, you can do work that matters, grow your career, and live a full life. We offer:

  • Career Development: Opportunities to build the career you dream of at a global company.

  • Health & Wellness: Free medical coverage (HIP PPO) for employees starting the next calendar year.

  • Retirement Savings: Excellent plan with high employer contribution.

  • Education Benefits: Tuition reimbursement, Freedom 2 Save student debt program, and FreeU bachelor’s degree program.

  • Recognition: Named one of the most admired companies in the world by Fortune, and recognized globally as a best place to work for diversity, working mothers, female executives, and scientists.


The Opportunity

We are seeking a Sr. Statistical Analyst I to independently contribute to statistical programming and analysis for clinical studies. This role involves close collaboration with biostatisticians, clinical teams, and regulatory functions, with opportunities to mentor junior programmers.


Key Responsibilities

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

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

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

  • Support regulatory submissions, DMC/CEC meetings, IRB packages, and publications.

  • Provide statistical expertise and interpret results for stakeholders.

  • Manage programming environments, study folders, and macros.

  • Mentor junior programmers, providing technical guidance and troubleshooting.

  • Ensure compliance with QMS, EMS, and regulatory standards.

  • Document datasets, programs, and specifications thoroughly.

  • Respond to ad hoc programming requests and complex data checks.

  • Communicate issues and escalate risks promptly.


Required Qualifications

  • Education:

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

    • Bachelor’s degree with 5+ years’ experience.

  • Extensive experience with clinical trial data analysis and SAS programming.


Preferred Qualifications

  • Advanced degree (M.S./Ph.D.).

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

  • Prior work in a highly regulated medical device environment.

  • Strong multitasking and project management skills under tight deadlines.

  • Excellent verbal and written communication skills.

  • Ability to explain complex procedures clearly and concisely.

  • Strong organizational skills, attention to detail, and leadership abilities.


Compensation

  • Base Pay Range: $75,300 – $150,700 (location-specific variations may apply).


Benefits

Learn more about our health and wellness programs at: www.abbottbenefits.com


Equal Opportunity

Abbott is an Equal Opportunity Employer, committed to diversity and inclusion.


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