Associate Statistical Analyst

Abbott

Last Updated: 11/14/2025 12:52:39 AM

Position Closed

Live Market Data for this Exact Role

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Current Days Open
7
Reqs Seen
2
Current Min Salary
$75,700.00 (Yearly)
Current Max Salary
$124,000.00 (Yearly)
Historical Time to Fill
7
First Seen
11/8/2025
Lowest Min Salary Seen
$75,700.00 (Yearly)
11/14/2025
Highest Max Salary Seen
$124,000.00 (Yearly)
11/14/2025

Full Job Description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Job Description Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Youll also have access to: Career development with an international company where you can grow the career you dream of Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelors degree A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists THIS POSITION IS AN ON-SITE DAILY ROLE. THIS POSITION CAN BE BASED OUT OF OUR FACILITY IN MAPLE GROVE, MN OR SANTA CLARA, CA The Opportunity We are seeking an Sr Statistical Analyst I to join our Biometrics team for Abbott Medical Devices. Independently, the Sr Statistical Analyst I will review study protocol, statistical analysis plans, CRFs and edit check specifications; work with biostatisticians and clinical staff to generate analysis datasets, data tables, figures and listings; write and document programs; perform ad hoc programming; and perform QC tasks. May lead a small programming team with 1-3 analysts on a project. What Youll Work On 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. Collaborate closely with cross-functional teams to develop ADS specifications and mock shells, in alignment with the team. Collaborate with clinical, regulatory, and data management teams to define data checking requirements and resolve discrepancies. Support regulatory submissions, DMC/CEC meetings, IRB packages, and scientific publications with statistical deliverables. Summarize statistical methodologies and interpret results for internal and external stakeholders. Set up programming environments, manage study folders, and create or modify project-specific macros. Provide statistical expertise to cross-functional teams and departments outside of Biostatistics as needed. Lead or mentor junior programmers, providing technical guidance and troubleshooting support. Ensure compliance with Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory standards. Respond to ad hoc programming requests and perform complex data checks for data management. Maintain detailed documentation of datasets, programs, and specifications. Communicate effectively with study teams and escalate critical issues to management in a timely manner. Required Qualifications Associates Degree (± 13 years) Minimum 1 year experience Preferred Qualifications M.S. degree in statistics, biostatistics or related majors with 3+ years minimum experience in statistical or SAS programming, OR Bachelor's degree with 5+ years experience. Extensive experience in clinical trial data analysis and SAS programming Advanced degree 2-5+ years experience in medical device or pharmaceutical clinical research studies. Experience working on medical device clinical studies in highly regulated environment. Ability to manage multiple projects and deliver high-quality results under tight timelines. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multitasks, prioritizes and meets deadlines in timely manner. Able to describe complex procedures concisely and accurately. Strong organizational and communication skills, attention to detail, and team leadership skills. The base pay for this position is $75,700.00 $124,000.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY: Clinical Affairs / Statistics DIVISION: MD Medical Devices LOCATION: United States > Santa Clara : Building A - SC ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions across the spectrum of health, around the world, for all stages of life. Whether its next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of lifes greatest health challenges. We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube Twitter

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