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ICON plc · 3 days ago

Biostatistician II

United States

Full-time

Remote

Mid Level

3+ years exp

ICON plc is a world-leading healthcare intelligence and clinical research organization, seeking a Biostatistician II to join their Data Monitoring Committee (DMC) team. In this role, you will collaborate with multiple sponsors providing unblinded DMC support across a diverse portfolio of studies, while writing statistical analysis plans and presenting statistical outputs during DMC meetings.

Biotechnology

H1B Sponsor Likely

Responsibilities

Writing DMC statistical analysis plans and designing statistical tables and figures for DMC reports

Presenting analysis plan and statistical outputs during DMC Organizational Meetings

Attending open and closed sessions of DMC data review meetings; present unblinded statistical summaries during closed sessions

Write data quality control specifications and utilize relevant computer languages (SAS, R) and software

Develop and execute analysis programs for interim analyses

Assist in conducting statistical analyses and interpreting results

Prepare summary reports of statistical tables and figures for DMC members

Review and document analysis and programming work for audit trail purposes

Work within documented standards and maintain project-specific biostatistics files

Collaborate effectively with ICON project team members, including data management, statistical programming, and clinical research personnel

Maintain a diverse portfolio of 10-15 individual studies across sponsors and therapeutic areas

Lead statistical programmers in preparation of statistical outputs

Embrace ICON's values, culture of process improvement, and commitment to client needs

Qualification

SASRBiostatisticsStatistical analysis plansStudy designEffective communicationOrganizational skillsCollaboration skillsTime management

Required

Bachelors, Masters or Ph.D in Biostatistics, Statistics, or a related field

3+ years of Biostatistics experience in clinical research (either at a CRO or sponsor)

Proficiency in statistical concepts, study design, sample size calculations/recalculations, and patient randomization procedures

Familiarity with statistical analysis plans and the design of statistical tables, figures, and data listings in regulated clinical trial environment

Advanced ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical studies simultaneously

Strong organizational skills and ability to prioritize with strong time management skills

Effective communication and collaboration skills to work with global, cross-functional teams and external clients

Benefits

Various annual leave entitlements

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

Life assurance

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Company

ICON plc

Glassdoor3.7

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.

Founded in 1990

Dublin, IE

10001+ employees

http://www.iconplc.com

H1B Sponsorship

ICON plc has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Trends of Total Sponsorships

2025 (4)

2024 (4)

2023 (5)

2022 (11)

2021 (4)

2020 (5)