Senior Statistician

Abbott Laboratories • Alameda, CA

5d • $90,000 - $180,000 • Onsite

About The Position

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. You’ll also have access to:
Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.
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

Requirements

• B.S. in statistics or Mathematics.
• MS/MA with 5+ years of related work experience or PhD with 3+ years of related work experience preferred

Responsibilities

• 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
• 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
• 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
• 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
• 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
• 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
• 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.
• Effectively mentors nonstatistical peers with regard to basic statistical methodology and departmental operations.
• Provides appropriate background, motivation, and training to less experienced statisticians.
• Can direct the activities of 1-2 statisticians by appropriately delegating assignments and reviewing work so projects are delivered on time with suitable quality.
• Interacts effectively with support staff (e.g., programmers and technical support specialists).
• Responsible for presenting to Senior management outcomes, status updates, and to bring to the attention of management if there are delays and where additional information/resources are needed.

Benefits

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees