Do you have good experience of programming via SAS, knowledge and experience of CDISC standards and are looking for a new and exciting challenge? If so, we are looking to recruit Senior SAS Programmers who can really make a difference to our company, employees, and customers. We are looking for individuals to support our global programming team. In exchange, we will provide a very competitive salary and wider benefits, with the opportunity to grow and develop your career. You will be joining one of the market leading companies focused on providing data related services to the pharmaceutical industry. As an award-winning, fast-growing company you will be working in an exciting environment that will offer you future growth and an opportunity to take on new responsibilities. This role can be completely remote or based from one of our local hubs. Deliver excellent customer care in support of genuine value and a great customer experience. Comprehensive knowledge of clinical and pharmaceutical drug development and associated ICH/GCP guidelines. Good knowledge of pharmaceutical industry standards Comprehensive understanding of current Quanticate, and client-specific standard operating procedures (SOPs) and processes, as well as applicable regulatory requirements and/or guidelines on behalf of the client. Provide mentoring in area of technical expertise. Ability to work with different, functions, and across sites, as required. Ability to review clinical documents, e.g. protocol, CRF and SAP. Perform other reasonable programming tasks as requested by management. Follow appropriate Project Management procedures. Work to the appropriate standards of the project. Demonstrated SAS programming knowledge to an advanced level with expected results in SAS competency test. Ability to work independently as a programmer. Provide programming expertise and support within the function on programming standards, processes and procedures. Qualified to degree level or equivalent, preferably in a numerate discipline. Understanding of basic statistics. Knowledge and experience on pharmaceutical industry and requirements for delivery of clinical trials. Preferably have programming experience covering activities from study set-up to final reporting. Should have PC skills, good knowledge of statistical software packages (particularly SAS), good organisational skills, good communication skills (oral and written), excellent analytical skills, works well as part of a team, and has a continuous improvement mentality and a good attention to detail.