As a PrincipalStatistical Programmer you will be dedicated to one of our global pharmaceutical clients; As a PrincipalStatistical Programmer you will be dedicated to one of our general pharmaceutical clients; The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.

Xml files for multiple studies Develop SAS programs which generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines Understand and follow FDA regulations which affect the reporting of clinical trial data. Participate in the development of CRFs,



edit check specifications, and data validation plans Provide review and/or author data transfer specifications for external vendor data CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. At a minimum bachelor's degree in computer science, data science, mathematics, or statistics major preferred ~7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or with a similar team and experience supporting drug development, medical device development, or intervention studies ~ Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment ~ Xml), medical terminology, clinical trial methodologies, and FDA/ICH regulation ~ Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities ~ Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support.

Prior work experience with pharmacokinetic data and the neuroscience field, proficiency in languages or tools other than SAS and R (e.Python, and Java, Shiny, Markdown, Unix/Linux and git)

📌 Senior/Principal Statistical Programmer Fsp (La Mancha)
🏢 Cytel
📍 La Mancha