Associate Statistical Analyst

Abbott • Full-time • United States > Santa Clara : Building A - SC, United States of America • 2d ago

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. 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 student debt program and FreeU 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 Ito 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

Associates Degree (± 13 years)

Minimum 1 year experience

Preferred Qualifications

M.S. degree in statistics, biostatisticsor 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:

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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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