Senior Statistical Analyst - RWE - SAS programming

• Develop and validate analysis datasets, tables, listings and figures.
• Apply programming standards and specifications consistently.
• Perform quality control and resolve data or programming issues.
• Collaborate with biostatistics, data management and clinical stakeholders.
• Maintain traceable programming documentation and submission readiness.
• Provide technical guidance, peer review or mentoring on complex work within the discipline., * 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 (https://careers.iconplc.com/benefits) 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.

• Degree in statistics, mathematics, computer science or related quantitative discipline, or equivalent relevant programming expertise.
• Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry.
• Proficiency in statistical software SAS (R or Python are also used in a more limited capacity)
• Understanding of clinical trial design, statistical methodologies, and regulatory requirements.
• Practical statistical programming experience in clinical trials using SAS or another appropriate statistical programming environment.
• Knowledge of CDISC SDTM and ADaM standards.
• Understanding of clinical trial data, statistical outputs and validation practices.
• Experience developing and validating analysis datasets, tables, listings and figures.
• Experience reviewing colleagues’ work and providing technical guidance on clinical statistical programming., * Experience supporting regulatory submissions.
• SAS programming capability (R or Python are also used in a more limited capacity)
• Advanced CDISC or Define XML expertise.

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.

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.