Biostatistician II

ICON plc

. Serve as lead biostatistician for programs of studies, or on simple to complex individual studies .

Posted 11/3/2026full-timeRemote • Pennsylvania • United States, MexicoJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in biostatistics and statistical analysis, with proficiency in SAS and R for conducting inferential statistics. Possesses strong knowledge of clinical trial methodologies and regulatory requirements, complemented by effective communication and leadership skills.

Highest-signal resume keywords

Biostatistical ExperienceSAS ProgrammingStatistical Analysis Plans (SAPs)Clinical Trials MethodologyMaster's Degree Or Ph.D In Biostatistics

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical AnalysisInferential StatisticsStudy DesignsStatistical MethodsStatistical Software PackagesData AnalysisStatistical ReportingClinical ResearchRegulatory RequirementsBiostatistics

Soft Skills

Effective CommunicationLeadership AbilityTime ManagementPrioritization Skills

Tools & Technologies

SASR

Industry Keywords

CROPharmaceuticalBiotechTherapeutic AreasClinical Trials

About the role

Key responsibilities & impact

Serve as lead biostatistician for programs of studies, or on simple to complex individual studies
Oversee statistical activities that support ICON’s interactions with clients and regulatory agencies
Review and approve statistical methods sections of study protocols
Author statistical analysis plans (SAPs) and statistical input to reports
Program using SAS and/or R for inferential statistics
Conduct statistical analyses for clients

Requirements

What you’ll need

Master's degree OR Ph.D in Biostatistics, Statistics, or a related field
1+ years of biostatistical experience in either a CRO, pharmaceutical, or biotech company
In-depth knowledge of study designs, and statistical analysis conventions in one or more therapeutic areas
Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages, including SAS
Experience working in a clinical research organization (preferred)
Effective written and verbal communication skills with demonstrated leadership ability
Ability to prioritize with strong time management skills
Legal right to work in the country where the role is based

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways