Senior Biotatistician
Senior Biotatistician
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$ 86700 - 173300
1 Vacancy
Job Description
JOB DESCRIPTION:
Sr. Biostatistician
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:
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical 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 bachelors 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. Biostatistician 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
- 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).
- Indicate the reporting relationships products budgets throughput level and purpose of contacts (internal and external) or other scope measures that are key to this position.
- Position interacts with customers from throughout the division.
- Often required to reconcile multiple and potentially conflicting priorities.
- Effective communication with various levels of personnel is required regularly.
- 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.
Required Qualifications
- 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
The base pay for this position is
$86700.00 $173300.00In specific locations the pay range may vary from the range posted.
JOB FAMILY:
Clinical Affairs / Statistics
DIVISION:
ADC Diabetes Care
LOCATION:
United States > Alameda : 1360-1380 South Loop Road
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
No
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Continuous standing 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: EEO is the Law link - Espanol: Experience:
Senior IC
Employment Type
Full-Time
Key Skills
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