Statistical Programmer Ii

hace 2 meses

Madrid, España Icon Clinical Plc A tiempo completo

.Statistical Programmer II, EMEAICON 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 developmentAt 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 medical device and 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 Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects. Project responsibilities include study design and case report form review, 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.You will have strong demonstrable experience in:
- Designing, developing, validating and documenting SAS programs to generate analysis datasets, generate summary tables, figures and listings.
- Support statisticians in the development and review of Statistical Analysis plans and programming specifications
- Responsible for assisting data management with implementing CRFsWe are looking for:
- Bachelors or Master's degree in statistics, biostatistics, or related field
- SAS Programming experience – (ideally 3 yrs or more)
- Major experience in the Pharmaceutical/CRO industryBenefits 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

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