Senior Non-Clinical Biostatistician

This is a fully remote position, open to applicants in United States.

📋 Description

• Engage in the development, validation, and support of genomic biomarker assays.

• Assist in the design of experiments and the formulation of study protocols.

• Conduct data analysis and establish methods for process oversight.

• Compile and prepare study reports.

• Act as a subject matter expert for regulatory submissions.

• Collaborate with various cross-functional departments.

• Choose and modify statistical techniques for specific aims using independent judgment.

• Partner with statistical collaborators.

• Utilize both theoretical and applied statistics.

• Employ SAS, R, Python, and other industry-standard analysis software.

• Design, analyze, report, and internally publish findings related to analytical validation and process monitoring.

• Work alongside scientists, pathologists, oncologists, as well as commercial, legal, and business development teams.

• Adhere to and support the company's Quality Management System policies and procedures.

• Maintain consistent and dependable attendance.

⛳️ Requirements

• Master’s degree in Biostatistics or a related field as specified in the key responsibilities.

• Over 6 years of relevant experience.

• Professional expertise in both theoretical and applied statistics.

• Strong programming capabilities in SAS, R, or Python.

• Proven proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint.

• Excellent verbal, written, graphical communication, and presentation abilities.

• Capacity to seek and incorporate feedback in a professional manner.

• Ability to work autonomously, prioritize tasks, and deliver high-quality outcomes.

• Skill in effective collaboration within a cross-functional team.

• Capability to perform essential duties with or without accommodations.

• Authorization to work in the United States without the need for sponsorship.

• Preferred: PhD in Biostatistics or over 9 years of relevant experience.

• Preferred: Statistical experience in molecular diagnostics, drug, or medical device development.

• Preferred: Experience in oncology.

• Preferred: Background in developing products for regulatory approval, such as by the FDA.

• Willingness to travel between Abbott Cancer Diagnostics locations.

• Ability to travel up to 5% of working time, which may include overnight or weekend travel.

🏝️ Benefits

• Opportunities for career development within an international company.

• Complimentary medical coverage in the Health Investment Plan (HIP) PPO medical plan for eligible employees in the upcoming calendar year.

• Exceptional retirement savings plan with a substantial employer contribution.

• Tuition reimbursement program.

• Freedom 2 Save student debt initiative.

• FreeU education benefit.

• Chance to obtain a bachelor’s degree through the FreeU education program.

• Recognition as a desirable workplace and a highly respected company.