Senior Statistical Programmer

ICON; Reading; On-site; GBP 100,000 - 125,000; Full time

Job summary

A leading clinical research organization in the United Kingdom is seeking a Senior Statistical Programmer II. This role involves designing and validating SAS programs for the analysis of clinical trial data, working closely with biostatisticians and ensuring compliance with regulatory standards. The ideal candidate will have a relevant degree and significant experience in statistical programming within the clinical research industry. This opportunity offers competitive salary and diverse benefits to promote work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• Significant experience in statistical programming within the clinical research or pharmaceutical industry.
• Strong proficiency in SAS programming and understanding of statistical methodologies.
• Excellent analytical skills and attention to detail.

Responsibilities

• Design and validate SAS programs for clinical trial data analysis.
• Collaborate with biostatisticians to develop analysis plans.
• Perform quality control checks on statistical outputs.

Skills

SAS programming

Statistical analysis

Quality control

Analytical skills

Communication skills

Education

Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science

Job description

Senior Statistical Programmer

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 II to join our diverse and dynamic team. As a Senior Statistical Programmer II at ICON, you will play a vital role in the analysis and reporting of clinical trial data, ensuring the integrity and accuracy of statistical outputs. You will contribute to the advancement of our clinical studies by developing and validating complex statistical programs, collaborating closely with biostatisticians, and adhering to regulatory standards.

What You Will Be Doing:

• Designing, developing, and validating SAS programs for statistical analysis and reporting of clinical trial data.
• Working closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods.
• Performing quality control checks and reviewing statistical outputs to ensure compliance with project specifications and regulatory guidelines.
• Assisting in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs.
• Mentoring junior programmers and contributing to team development by sharing best practices and technical knowledge.

Your Profile:

• Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field.
• Significant experience in statistical programming within the clinical research or pharmaceutical industry.
• Strong proficiency in SAS programming and a solid understanding of statistical concepts and methodologies.
• Excellent analytical skills, attention to detail, and the ability to manage multiple projects simultaneously.
• Strong communication and interpersonal skills, with the ability to work collaboratively within a multidisciplinary team.

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, 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.

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