Senior Biostatistician job opportunity at Abbott.



DateMore Than 30 Days Ago bot
Abbott Senior Biostatistician
Experience: 5-years
Pattern: full-time
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loacation United States - California - Santa Clara, United States Of America
loacation United States ..........United States Of America

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:   About Abbott   Abbott is a global healthcare leader, creating breakthrough science to improve people’s health.   We’re   always looking towards the future,   anticipating   changes in medical science and technology.   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’l l 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 ONSITE DAILY ROLE.   We are looking for a Senior Biostatistician for either our Maple Grove, MN, Santa Clara, CA or   Burlington, MA locations.   The Opportunity   We are seeking an experienced, high caliber Senior Biostatistician to join Abbott’s medical   device   clinical research organization. This position includes providing statistical expertise in clinical   study design, writing statistical analysis plans and reports, performing statistical analysis and   programming, checking data quality, preparing analysis datasets,   generating   and/or validating   data listing, and tables/reports. This position will also assist on additional study projects or tasks   which may arise.     Working under limited supervision by the statistical manager, provides statistical support to   clinical study teams and external teams. This includes:   statistical input into clinical study designs, endpoints, hypotheses tests and sample   size calculations   performing statistical analysis of clinical study data   validating statistical a nalyses co nducted by statistical peers or colleagues.   This position may also perform statistical analysis or provide statistical input on other projects as   assigned by the statistical manager. Able to provide significant input into complex clinical study   designs   What   You’ll   Work On   Job Duties:   Provide statistical input into clinical study design, endpoints, hypotheses tests and   sample size calculations   Write statistical sections of protocols   Write statistical analysis plans   Provide input into data collection forms (Case Report Forms) and data management   plan   Provide input on study processes, especially those affecting scientific integrity and   data quality   Write or provide input into Data Monitoring Committee (DMC) and/or Clinical Events   Committee (CEC) charter   Ensure scientific integrity and data quality of clinical trials are preserved   Participate in DMC meetings as appropriate   Prepare statistical reports or statistical sections of clinical study reports   Interpret statistical results   Generate line listings for regulatory reporting as appropriate   Perform validation of statistical analyses conducted by statistical peers or colleagues   Ensures accuracy of report text and consistency between summary tables in the body   of reports and the corresponding statistical tables and listings.   Responsible for statistical methods   Identifies   and corrects common flaws in interpretation of results, inconsistency in   presentation or inference, and adherence to Abbott report guidelines.   Provides meaningful input to the development of a report strategy.   Works collaboratively with peers to develop quality protocols, CRF, schema, and   reports per agreed timelines.   Provides   accurate   and   timely   answers to routine questions from clients, scientific   insight when answering nonstandard questions, and independently pursues analyses   suggested by the data.   Communicates an understanding of basic clinical principles for his/her project and   acts   in accordance with   those principles.   Can clearly communicate basic statistical concepts to other scientists and   nonscientists. Informs supervisor or manager on   important issues   in a timely manner .   Required Qualifications:   Masters in statistics or biostatistics with a minimum of 5 years of experience or Ph.D. in statistics or biostatistics with 3 years of experience.   Able to write/describe statistical models of moderate complexity.   Extensive experience with SAS is   required ; experience with R,   Winbugs , JMP, NCSS   PASS   and other statistical software are a plus.   Knowledge of Bayesian and/or adaptive design methods and data mining are a plus.   Bachelors   Degree (± 16 years), BS/BA with 5+ years related work experience OR an equivalent combination of education and work experience,    Masters   Degree (± 18 years), MS with 3+ years of related work experience OR an equivalent combination of education and work experience   Preferred Qualifications:   Masters in statistics or biostatistics with a minimum of 5 years of experience or Ph.D.   in statistics or biostatistics with 3 years of experience.   Able to write/describe statistical models of moderate complexity.   Extensive experience with SAS is required; experience with R, Winbugs, JMP, NCSS   PASS and other statistical software are a plus.   Knowledge of Bayesian and/or adaptive design methods and data mining are a plus.   Minimum of 5 years of experience in medical device Clinical Research role is   preferred.   WHAT WE   OFFER   :   At Abbott, you can have a good job that can grow into   a great   career .   We offer:   A fast-paced work environment where your safety is our priority   Training and career development, with onboarding programs for new employees and   tuition   assistance   Financial security through competitive compensation,   incentives   and retirement plans   Health care and well-being programs including medical, dental, vision,   wellness   and   occupational health programs   Paid time off   401(k) retirement savings with a generous company match   The stability of a company with a record of strong financial performance and history of   being actively involved in local communities   * 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.         The base pay for this position is $86,700.00 – $173,300.00 In specific locations, the pay range may vary from the range posted.       JOB FAMILY: Clinical Affairs / Statistics       DIVISION:          LOCATION: United States > Santa Clara : Building A - SC       ADDITIONAL LOCATIONS: United States > Maple Grove : 6820 Wedgwood Road N.       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

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