About the role At ICON, its 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. Thats our vision. Were driven by it. And we need talented people who share it. If youre as driven as we are, join us. Youll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and youll 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 Please use the below link for job application and quicker response.https://lifelancer.com/jobs/view/3acb0d59deb3bdfa28e888a8e4149a82