ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs, collaborating with biostatisticians, and ensuring compliance with regulatory standards.
ICONの Senior Statistical Programmer I として、臨床試験データの解析および統計解析プロセスを支援し、高品質な成果を確実にする上で重要な役割を担っていただきます。
統計プログラムの開発・検証、バイオスタティスティシャンとの協働、規制基準への準拠などを通して、臨床試験の成功に貢献していただきます。
What You Will Be Doing:
- Developing and validating SAS programs for statistical analysis and reporting of clinical trial data.
- Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.
- Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting.
- Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions.
- Contributing to process improvements by identifying efficiencies in programming practices and methodologies.
- 臨床試験データの統計解析およびレポート作成のための SASプログラムの開発・検証
- バイオスタティスティシャンと協働し、解析計画やデータに適用する統計手法を定義
- 統計アウトプットの 品質管理（QC） を実施し、精度・一貫性を確保
- 規制当局向け提出資料に含まれる統計レポート、プレゼン資料、出版物の準備を支援
- プログラミング手法やプロセスの改善につながる効率化の提案
Your Profile:
- Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field.
- Experience in statistical programming, preferably in a clinical research or pharmaceutical setting.
- Strong proficiency in SAS programming, with a solid understanding of statistical concepts and methodologies.
- Excellent analytical and problem-solving skills, with a keen attention to detail.
- Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information.
- 統計学、数学、コンピュータサイエンス、または関連分野の 学士または修士号
- 統計プログラミングの経験（臨床研究または製薬業界での経験があれば尚可）
- SASプログラミングに精通し、統計の概念・手法に対する確かな理解を有していること
- 優れた分析力・問題解決能力を持ち、細部への注意力が高い方
- チーム環境で協働し、複雑な情報をわかりやすく伝える 高いコミュニケーション力 を持つ方
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Skills Required
- Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related field
- Experience in statistical programming, preferably in clinical research or pharmaceutical setting
- Strong proficiency in SAS programming with understanding of statistical concepts
- Excellent analytical and problem-solving skills
- Strong communication skills
ICON plc Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.
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Healthcare Strength — Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
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Leave & Time Off Breadth — Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
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Retirement Support — Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.
ICON plc Insights
What We Do
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. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
