.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.General Summary for Biostatistician I:Designs, plans, and executes biostatistical components of clinical studies. Uses sound statistical methodology to conduct studies, prepares the statistical components of protocols, and is responsible for the statistical components of reports.Primary Responsibilities:- Applies knowledge of statistical methodology to ensure proper implementation of clinical studies- Provides statistical oversight across the whole clinical study. Develops statistical analysis plans and reporting specifications for clinical studies- Contributes to clinical study protocols and clinical study reports. Reviews reports and underpins the results with statistical expertise- Accountable for the quality and delivery of the table, figure, and listing (TFL) packages- Analyzes and interprets results from clinical studies using sound statistical methodologyBiostatistician I Role and Responsibilities:- Contributes to the development of statistical analysis plans including TFL shells- Performs statistical analyses under the guidance of other statisticians or independently for simple clinical studies- Assists with the review of TFLs, tabulation datasets, and derived datasets- May assist with the development and review of CRFs and edit specifications- May serve as lead biostatistician for simple clinical studies- Working knowledge of multiple statistical and therapeutic areas, the drug development process, SAS procedures, and good programming practices- Ability to plan, implement, and monitor the statistical processes for clinical studies- Good written and oral communication skills- Problems are varied and non-routine. Uses previous experience to identify most appropriate solution. Work is performed under general guidance and direction- Interprets or explains data or information to deliver messages. Requires objective review of difficult work problems, obtaining cooperation or approval- Contributes to the achievement of goals through personal effort and influence over others