Associate Biostatistician

Associate Statistician GRADE 14

About Abbott

Abbott is a global healthcare leader creating breakthrough science to improve peoples health.Werealways looking towards the futureanticipatingchanges 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.Youllalso 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 andFreeUeducation benefit - an affordable and convenient path to getting a bachelors degree.

• A company recognized asa great placeto 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 an Associate Biostatistician for either our Maple Grove MN Santa Clara CA or Burlington MA locations.

The Opportunity

We are seeking an experienced high caliber Biostatistician to join Abbotts 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 supervision by the statistical manager provides statistical support to clinical study teams and external teams.

Job Duties

- Responsible for comprehensive protocol review

- Responsible for assuring that data for statistical analysesareaccurate

STATISTICAL ANALYSES

-Assistsin the implementation of protocolmethodologyand statistical analysis plans

- Responsible for the accuracy and timeliness of statistical input into reports or decisions

- Responsible for computer programs that areaccurateefficientand well documented

-Demonstratesbasic understanding of statistical concepts and methodologies

SCIENTIFIC REPORTS AND PUBLICATIONS

- Responsible for accuracy of statistical tables and data listings and accuracy of report text

-Identifiesand corrects flaws in interpretation of results inconsistency in presentation or inference

CONSULTATION

- Providesaccurateandtimelyanswers to routine questions from clients and scientific insight when answering nonstandard questions

TRAINING SUPERVISION MENTORING

- Can provide formal training to non-statisticians

-Describeprimaryresponsibilities of this position.

-Responsible for implementing andmaintainingthe effectiveness of the quality system.

- Ensures accuracy of report text and consistency between summary tables in the body of reports andthecorresponding statistical tables and listings.

-Assistswith thedevelopment ofquality protocols CRF schema and reportsperagreed timelines.

- Providesaccurateandtimelyanswers to routine questions from clients

- Communicates an understanding of basic clinical principles for his/her project and acts inaccordancewiththose principles.

- Can clearly communicate basic statistical concepts to nonscientists.

- Informssupervisorormanageronimportant issuesin a timely manner.

Required Qualifications:

• BachelorsDegree( 16 years)Bachelors Degreein Statistics or related field

• Masters Degree or PhD Preferred

• Minimum 1 year experience