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.
Connect With Us
Website: www.abbott.com
Facebook: facebook.com/Abbott
Twitter: @AbbottNews, @AbbottGlobal
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