Associate Biostatistician

ICON plc

Associate Biostatistician at ICON, responsible for statistical analysis of clinical trial data and report generation. Collaborating with multidisciplinary teams to support innovative treatment development.

Posted 7/15/2026full-timeWarsaw • 🇵🇱 PolandJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in statistical analysis and methodologies for clinical trials, with a strong focus on data integrity and regulatory compliance. Proficient in statistical software and effective communication within multidisciplinary teams.

Highest-signal resume keywords

Master’s Degree In StatisticsStatistical AnalysisSAS SoftwareClinical Trial DesignStrong Analytical Skills

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Statistical AnalysisStatistical MethodologiesData ValidationQuality Control ProcessesStatistical ProgrammingAnalysis PlansRegulatory SubmissionsStatistical SummariesClinical ResearchAttention To Detail

Soft Skills

Excellent Communication SkillsCollaborative Work

Tools & Technologies

SAS SoftwareR Software

Industry Keywords

Clinical TrialsBiostatisticsRegulatory Guidelines

About the role

Key responsibilities & impact

Conducting statistical analyses and generating reports for clinical trials under the guidance of senior statisticians
Collaborating with clinical teams to design and validate statistical methodologies for trial protocols
Preparing and presenting statistical summaries and interpretations for regulatory submissions and internal meetings
Ensuring data integrity and accuracy through rigorous statistical validation and quality control processes
Assisting in the development of statistical programming and analysis plans in accordance with regulatory guidelines

Requirements

What you’ll need

Master’s degree in Statistics, Biostatistics, or a related field
Experience with statistical software such as SAS (highly preferable), R, or similar tools
Understanding of clinical trial design and statistical methods applicable to clinical research
Strong analytical skills with a keen attention to detail and accuracy
Excellent communication skills and the ability to work collaboratively within multidisciplinary teams

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