Senior Statistical Analyst I (on site)

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.

**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.

You’ll 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 (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU (https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html) education benefit - an affordable and convenient path to getting a bachelor’s 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 You’ll 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**

+ 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

**Preferred** **Qualifications**

+ 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.

**Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life.

Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is $75,300.00 – $150,700.00.

In specific locations, the pay range may vary from the range posted.

An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call 224-667-4913 or email corpjat@abbott.com

Required Skill Profession

Other General