What are the responsibilities and job description for the Statistical Analyst - Medical Devices position at Abbott?

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 : 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
Free medical coverage for employees
via the Health Investment Plan (HIP) PPO
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 a Statistical Analyst to join our Clinical Research team for Abbott Medical Devices. In this role, the Associate Statistical Analyst will provide statistical support to the Biostatistics Supervisor / Manager and the Cardiovascular Division (CVD) for clinical studies. This includes providing statistical expertise in statistical programming, checking data quality, preparing analysis datasets, generating and / or validating data listing, and tables / reports as well as performing statistical analysis and preparing statistical analysis plans. This position will also assist on additional study projects or tasks which may arise.

What You'll Work On

Work with Biostatistics Supervisor / Manager, clinical or regulatory staff in contributing or preparing statistical section of protocols

Assist in data collection forms, writing statistical analysis plans, performing sample size and / or power calculations as appropriate.

Create randomization, sampling, and other study tools.

Work with Biostatistics Supervisor / Manager, data management group or clinical study teams to identify the necessary data checking listings or reports (e.g. weekly, biweekly, or ad hoc)

Write SAS programs to create reports, handle moderately complex SAS programming issues as well as other related programming issues.

Performs quality check of the SAS datasets against the source data provided

Validate SAS programs, analysis data and results

Help study team (CRAs, monitors, etc.) on utilization of data checking reports

Work with Biostatistics Supervisor / Manager and study team to determine the timelines.

Define programming constraints and the contents of the statistical tables and reports, including necessary explanation of data and analysis.

Identify outstanding data errors and work with clinical study teams to ensure the up-to-date and error free data are available at the time of analysis.

Prepare datasets for statistical analysis.

Generate and / or validate patient data listings, statistical analysis summary tables and reports for the

regulatory Annual Reports and submissions, DMC / CEC meetings, investigator institutional review boards (IRBs), conferences, etc.

Write statistical analysis methodology summary or sections, review summary reports and interpretations to the reports

Create, document, and maintain detailed data definition and inventory of all data and program.

Work with Biostatistics Supervisor / Manager to determine statistical project assignments.

Reading statistical analysis and clinical study papers and publications

Compiles clinical data and relevant background material of the studies for the Biostatistics Supervisor / Manager or study team for review.

Provide statistical analysis support in the publication and presentation of investigator projects.

Provide statistical expertise to departments outside of CVD as appropriate, including assisting in the analysis and interpretation of statistical data.

Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

Serve as a back-up for other biostatistician(s)

Required Qualifications

M.S. degree in statistics, biostatistics or related majors with 2 years minimum experience in statistical or SAS programming, OR Bachelor's degree with 2-5 years' experience will be considered as well.

SAS Experience is REQUIRED .

Knowledge of at least one database software package required.

Preferred Qualifications

Advanced degree

2-5 years experience in medical device or pharmaceutical clinical research studies.

Statistical knowledge and extensive SAS skills (i.e., proven experience in SAS coding).

Experience working on medical device clinical studies in highly regulated environment.

Ability to work within a team and as an individual contributor in a fast-paced, changing environment.

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 skills, attention to detail, and financial / business acumen

Apply Now

Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives : www.abbottbenefits.com

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

57,300.00 - $114,700.00

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

JOB FAMILY :

Clinical Affairs / Statistics

DIVISION : AVD Vascular

LOCATION : United States >

Maple Grove : 6820 Wedgwood Road N.

ADDITIONAL LOCATIONS :

United States >

Santa Clara : Building B - SC

WORK SHIFT : Standard

TRAVEL :

Yes, 10 % of the Time

MEDICAL SURVEILLANCE :

SIGNIFICANT WORK ACTIVITIES :

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

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

Salary : $57,300 - $114,700

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