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.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. Youll also have access to:
The Opportunity
This Sr. Statistician role will be based out of our Alameda, CA location in the Tech Ops division.
PROTOCOLS INPUT, RANDOMIZATION SCHEDULE, AND DATABASE ACTIVITES
- Works with project team to decide on appropriate study design and statistical methodology
- Responsible for comprehensive protocol review
- Responsible for randomization schedule, sample size and power calculations
- Responsible for assuring that data for statistical analyses are accurate
STATISTICAL ANALYSES
- Responsible for implementation of protocol methodology and statistical analysis plans
- Responsible for the accuracy and timeliness of statistical input into reports or decisions
- Responsible for validity of alternative analysis strategies when changes to planned analyses are needed
- Responsible for computer programs that are accurate, efficient and well documented
- Demonstrates extensive understanding of statistical concepts and methodologies
SCIENTIFIC REPORTS AND PUBLICATIONS
- Responsible for Statistical Methods section
- Responsible for accuracy of statistical tables and data listings, and accuracy of report text
- Identifies and corrects flaws in interpretation of results, inconsistency in presentation or inference
- Provides significant and timely input to the development of a report strategy
CONSULTATION
- Works collaboratively with peers to develop efficient designs, quality protocols and reports per agreed timelines
- Provides accurate and timely answers to routine questions from clients, and scientific insight when answering nonstandard questions
- Responsible for maintaining good client relationships and developing strategies for expanding client base
- Communicates an understanding of product development and acts in accordance with those principles
- Effectively presents statistical concepts and arguments to management, regulatory agencies and scientists
- Provides meaningful and timely input in the development of a clinical program strategy
TRAINING, SUPERVISION, MENTORING
- Effectively mentors less experienced statisticians
- Can lead a team of statisticians and programmers on a particular clinical trial
- Can provide formal training to statisticians and non-statisticians
- Seen as a project leader on key initiatives
PROJECT COORDINATION AND REGULATORY ACTIVITIES
- Coordinates and leads the work of the section in multiple project areas ensuring that statistical support meets regulatory needs
- Effectively interacts with project leaders, and regulatory affairs.
- Responsible for the accuracy and appropriateness of statistical input (e.g., protocol design, statistical methodology, interpretation of results and inference) provided for regulatory submissions, discovery and development decisions
What Youll Work On
Required Qualifications
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.
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