Join Us at ICON: High-Impact Careers in Clinical Research

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our clients and help us fulfill our mission to advance and improve patients' lives.

Why Join ICON?

Our "Own It" culture is driven by four key values that unite us as individuals and distinguish us as an organization: Accountability, Delivery, Collaboration, Partnership, and Integrity. Our goal is to be the Clinical Research Organization that delivers excellence to our clients and patients at every touchpoint. We aspire to be the partner of choice in drug development.

We are driven by this vision, and we need talented people who share it. If you're as driven as we are, join us. You'll work in a dynamic and supportive environment with some of the brightest and friendliest people in the sector, helping to shape an industry.

About the Role: Senior Statistical Programmer II

We are the global biostatistics team dedicated to late-phase research, working on (but not limited to) peri and post-approval research, post-authorization safety studies, observational and non-interventional studies, patient-reported outcomes, as well as analyses for abstracts, papers, and manuscripts.

As a Senior Statistical Programmer II, you will be responsible for the statistical aspects of clinical and preclinical research projects. Your responsibilities will include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. You may also be required to coordinate analysis efforts across multiple research projects conducted for a client.

What We Need:

• Minimum of 3 years of industry experience in SDTM, ADAM TLF.
• Extensive programming experience in SAS or R.
• Experience with reporting clinical trials, including statistical data handling, analysis, and reporting.
• Experience with the review and documentation of programs.
• Good knowledge of drug development.
• Experience with clinical database technologies, data models, and advanced programming.
• Experience with collaboration across professional and regional borders.
• Regular experience with communication and presentations.
• In-depth knowledge of computer systems and IT.
• Good knowledge of GxP and guidelines within drug development.
• Basic understanding of the pharmaceutical industry and key elements of the value chain, with a focus on immediate stakeholders and how to deliver on own goals.

Additional Information:

Company Name: Lifelancer
Job Title: Biostatistician / Senior Statistical Programmer I & II