SAS Programmer for Regulatory Submissions Full-time Job

As a SAS Programmer for Regulatory Submissions, you will develop and maintain SAS programs to support regulatory submissions. Responsibilities include preparing datasets, tables, listings, and figures for submission to regulatory agencies such as the FDA and EMA. You will ensure compliance with regulatory standards and guidelines, perform data validation, and work with regulatory affairs teams to meet submission deadlines. Strong knowledge of regulatory requirements, SAS programming skills, and experience with clinical data submissions are essential. Attention to detail, the ability to manage multiple projects, and effective communication skills are required for this role.