Abbott
Statistical Analyst - Medical Devices
Abbott, Osseo, Minnesota, United States, 55311
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 AbbottAt 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 ofFree medical coverage for employees* via the Health Investment Plan (HIP) PPOAn excellent retirement savings plan with high employer contributionTuition reimbursement, the
Freedom 2 Save
student debt program and
FreeU
education benefit - an affordable and convenient path to getting a bachelor’s degreeA 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 FortuneA 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 scientistsTHIS POSITION IS AN ON-SITE DAILY ROLE.THIS POSITION CAN BE BASED OUT OF OUR FACILITY IN MAPLE GROVE, MN OR SANTA CLARA, CAThe OpportunityWe 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 OnWork with Biostatistics Supervisor/Manager, clinical or regulatory staff in contributing or preparing statistical section of protocolsAssist 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 providedValidate SAS programs, analysis data and resultsHelp study team (CRAs, monitors, etc.) on utilization of data checking reportsWork 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 theregulatory 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 reportsCreate, 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 publicationsCompiles 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
QualificationsM.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
QualificationsAdvanced degree2-5+ 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 acumenApply 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.comFollow 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:
Yes
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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf#J-18808-Ljbffr
Working at AbbottAt 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 ofFree medical coverage for employees* via the Health Investment Plan (HIP) PPOAn excellent retirement savings plan with high employer contributionTuition reimbursement, the
Freedom 2 Save
student debt program and
FreeU
education benefit - an affordable and convenient path to getting a bachelor’s degreeA 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 FortuneA 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 scientistsTHIS POSITION IS AN ON-SITE DAILY ROLE.THIS POSITION CAN BE BASED OUT OF OUR FACILITY IN MAPLE GROVE, MN OR SANTA CLARA, CAThe OpportunityWe 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 OnWork with Biostatistics Supervisor/Manager, clinical or regulatory staff in contributing or preparing statistical section of protocolsAssist 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 providedValidate SAS programs, analysis data and resultsHelp study team (CRAs, monitors, etc.) on utilization of data checking reportsWork 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 theregulatory 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 reportsCreate, 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 publicationsCompiles 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
QualificationsM.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
QualificationsAdvanced degree2-5+ 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 acumenApply 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.comFollow 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:
Yes
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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf#J-18808-Ljbffr