Senior Biostatistician

Thermo Fisher Scientific

. Function independently as a lead statistician with minimal oversight .

Posted 10/22/2026full-timeRemote • North Carolina • United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical analysis and project management, with a strong foundation in SAS and R programming. Capable of leading complex projects, mentoring team members, and ensuring compliance with departmental standards.

Highest-signal resume keywords

Masters In BiostatisticsSAS ProgrammingR ProgrammingProject ManagementStatistical Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical AnalysisSample Size CalculationAnalysis Database CreationStatistical Analysis MethodsClinical Trial DesignData InterpretationTable And Listing SpecificationsReport PreparationBudget MonitoringBusiness Development

Soft Skills

MentoringCommunicationOrganizational SkillsInterpersonal SkillsTime Management

Industry Keywords

Clinical TrialsSOP ComplianceProject Lead ExperienceClient Facing ExperienceStatistical Reporting

About the role

Key responsibilities & impact

Function independently as a lead statistician with minimal oversight
Deliver project statistician tasks, including analysis database creation, statistical analyses, and formatted statistical analysis tables and summaries
Mentor junior team members and provide project guidance and statistical advice
Ensure compliance with departmental SOPs and procedures
Lead complex projects and provide senior project review
Interact with sponsors and present to sponsors and regulatory agencies as needed
Review sample size calculations, protocols, clinical designs, statistical analyses, and randomization documentation
Write and review analysis plans and define appropriate statistical analysis methods and procedures
Review specifications and oversee development and maintenance of analysis databases
Oversee collaboration with programmers and data management personnel
Supervise creation of table and listing specifications
Prepare reports, manuscripts, and other documents
Contribute statistical methods sections for integrated clinical, safety, and efficacy reports
Monitor project budgets and communicate scope or budget changes to management and sponsors
Provide input on hiring recommendations, department policies, and resourcing requirements
Represent the department to other divisions
Assist with bidding and business development activities, including bids and timelines

Requirements

What you’ll need

Masters in Biostatistics, Statistics or Math at a minimum is required
An equivalency consisting of a combination of appropriate education, training and/or directly related experience may be considered sufficient
Previous experience comparable to 4+ years
Project lead client facing experience is required
Experience programming in SAS and R is required
Comprehensive SAS programming skills (BASE, STAT, MACRO and GRAPH)
Comprehensive understanding of a wide variety of clinical trials/designs and corresponding reporting of data
In-depth understanding of interpreting results from statistical analyses of complex data
Strong project management skills, including management of multiple projects
Excellent written and verbal communication skills, including proficiency in the English language
Substantial organizational, time management, and planning skills
Strong interpersonal skills and ability to work effectively in a team environment
Must be legally authorized to work in the US without sponsorship
Must be able to pass a comprehensive background check, including drug screening

Benefits

Comp & perks

Relocation assistance is NOT provided
Equal employment opportunity and affirmative action employer
Reasonable accommodation for individuals with disabilities
Accessibility service for job seekers requiring accommodations
Standard Monday–Friday work schedule