Abbott Senior Biostatistician in Plymouth, Minnesota
At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.
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 (1) statistical input into clinical study designs, endpoints, hypotheses tests and sample size calculations (2) performing statistical analysis of clinical study data (3) validating statistical analyses conducted 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
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.
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 strongly desired; 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.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call 224-667-4913 or email firstname.lastname@example.org