Ben has a high level of expertise in laboratory data within Clinical Trials, early phase environment, as well as in-depth knowledge of Laboratory Information Management Systems (LIMS). With this expertise, Ben has produced clinical laboratory data for a large range of clients, and is proficient in SOP writing, as well as computer system validation. As a senior standards consultant, Ben has a wealth of knowledge across industry data standards, such as CDISC SDTM, and has advanced SAS programming skills. In addition, Ben brings the benefit of related documentation knowledge, including change controls, qualification and validation plans, and incident reporting.