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The Clinical Biostatistician will collaborate with cross-functional teams to design clinical studies and develop evidence for molecular oncology tests. They will apply statistical methodologies to monitor data quality, conduct simulations, and communicate results for regulatory submissions and clinical reports.
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. 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 position is remote in the Cancer Diagnostics Division.
As the Clinical Biostatistician, you’ll have the chance to collaborate with interdisciplinary, cross-functional teams to develop and establish evidence for molecular tests for screening, diagnosis, prognosis, monitoring, and therapy selection in oncology.
Essential Duties Include, but are not limited to, the following:
Ability to apply strong verbal, written, and graphical communication/presentation skills.
Ability to work independently, prioritizing and producing high quality results.
Ability to collaborate effectively as part of a cross-functional team.
Maintain regular and reliable attendance.
Ability to act with an inclusion mindset and model these behaviors for the organization.
Under the direction of other statisticians, assist the biostatistical function on project-level work.
Provide input into the design of analytical validity, clinical validity, clinical utility, health economics, and clinical experience studies by:
Evaluating evidentiary requirements.
Contributing to proposals, FDA pre-submissions, and study protocols (selecting endpoints, power and sample size calculations, and analysis plans).
Reviewing case report forms and data transfer requirements.
Drafting statistical analysis plans.
Apply standard statistical methodology and programming to:
Monitor laboratory and clinical data quality.
Develop evidence for clinical predictive models in clinical studies and trials.
Conduct simulation studies.
Communicate statistical results in tables, figures, and listings; statistical analysis reports; clinical study reports; abstracts; manuscripts; regulatory submissions; presentations; and marketing collateral.
Evaluate investigator sponsored study designs and analysis plans, evidence developed for external molecular tests, and applicability of novel statistical techniques.
Ability to regularly seek and integrate feedback from team members and managers in a professional manner.
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
Support and comply with the company’s Quality Management System policies and procedures.
Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
Ability to travel up to 5% of working time away from work location, may include overnight/weekend travel.
Minimum Qualifications
Master’s degree in Biostatistics or related field as outlined in the essential duties.
Working knowledge of theoretical and applied statistics.
Strong statistical programming skills (SAS, R, or Python).
Basic computer skills to include internet navigation and email usage.
Working knowledge of Microsoft Office programs, such as Word, Excel, PowerPoint, Outlook, Access, OneNote, and Publisher.
Demonstrated ability to perform the essential duties of the position with or without accommodation.
Authorization to work in the United States without sponsorship.
Preferred Qualifications
2 years of relevant work experience.
Experience in developing products for approval by regulatory authorities such as FDA.
Experience in molecular diagnostic, drug, or medical device development; epidemiology; public health; or healthcare
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.
The base pay for this position is
$61,300.00 – $122,700.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
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