Biostatistician / Senior Statistical Programmer I & II

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.The role: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 Sr Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.

What we need:

• Minimum 3 years’ experience Industry experience in SDTM, ADAM & TLF.
• Extensive experience with programming in e.g. SAS or R
• Experience with reporting clinical trials, including statistical data handling, analysis and reporting
• Experience with 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

Benefits of Working in ICON:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON is an equal opportunity and inclusive employer and 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 through the form below.

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