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
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | Tarasadi | Vadodara | Vapi |Maharashtra :
Airoli | Ambernath | Amravati | Aurangabad | Dhule | Dombivali | Jalgaon | Kolhapur | Kurkumbh | Kurla | Madhapur | Mumbai | Nagpur | Nashik | Navi Mumbai | Pune | Pune city | Shirpur | Tandalja | Tarapur | Thane | Vikhroli | Yerawada |Haryana :
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Baddi | Solan |Rajasthan :
Banasthali | Bhiwadi | Jaipur | Pilani | Udaipur |Karnataka :
Bangalore | Belgaum | Bengaluru | B.G Nagara | Bommasandra | Colorado | Czech Republic | Karnataka | Mangaluru | Mysore | Udupi |Punjab :
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Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Albany | Biddle | Brooklyn | Buffalo | Hauppauge | Hawthorne | Hicksville | Ithaca | Middleburgh | Morningside Heights | New York | Pearl River | Poughkeepsie | Rensselaer | Rhinebeck | Syracuse | Utica | Watertown |New Mexico :
Albuquerque | Farmington | Santa Fe | Tucumcari |Pennsylvania :
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Anchorage | Barrow | Bethel | Juneau | Sitka | Wrangell |Massachusetts :
Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
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Bangor | Brewer |New Jersey :
Basking Ridge | Bloomfield | Branchburg Township | Bridgewater | Brunswick | Burlington | Charlotte | Clark | Cranbury | Dunellen | East Brunswick | Edison | Fairfield | Far Hills | Flemington | Hackensack | Hopewell | Indianapolis | Jersey City | Linden | Livingston | Lyndhurst | Mahwah | Monmouth Junction | Montville | Mount Arlington | Newark | New Brunswick | Nutley | Paramus | Parsippany | Passaic | Paterson | Peapack-Gladstone | Pine Brook | Piscataway Township | Plainsboro | Princeton Junction | Rahway | Raritan | Somerset | Somerville | South Plainfield | Sparta | Summit | Titusville | Trenton | Warren Grove | Westfield | West Orange | Wharton | Whippany |Ohio :
Batavia | Blue Ash | Cincinnati | Cleveland | Columbus, | Dayton | Erie | Evendale | Franklin | Hamilton | Huber Heights | Kings Mills | Macedonia | Mason | Milford | Montgomery | Norwood | Oregoina | oxford | Waynesville |LA :
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Duluth | Eden Prairie | Fridley | Hibbing | Maple Grove | Minneapolis and St. Paul, Minnesota. | Minnetonka | St.Paul |Kentucky :
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Bishop | Melbourne | Switzerland | Nairobi | Slovakia | Lenexa | Xzagreb | Blue Bell | Regulatory Labeling Manager (NA and LATAM Only) | Remote - Europe | Green Way | Remote, USA | Texas | Ireland | Springville | Hammond | Remote - South America (Latin Americal) | Zaragoza | Minnesota | Remote | Medan | French | Tulsa | Hungary | Faridabad | Remote - Middle East | Victoria | Lousiana | Thailand | Remote - Africa | Manipal | Castlebar | Riga | Leinster | Belgium | Bountiful | McFarland |Republic of Colombia :
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Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
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Midrand | South Africa |Nišava District :
Niš |Bohemia :
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Sarajevo |Singapore :
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