Principal Statistical Programmer - Sponsor Dedicated, EMEA

Job description

This role is for upcoming future opportunities that may arise at Fortrea. As a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex projects for a renowned, innovative and global top pharmaceutical company. You will be involved in liaising with the entire study team as needed, including Clinical, Medical Writing, Safety and Biometrics. It is a great opportunity to see more how this works from a Big Pharma perspective, whilst still being part of a global CRO with opportunity for future career growth. This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas. You can be 100% home-based in EMEA or you can work from our local office in your home country. Your Responsibilities: Plan, execute and oversee all programming activities on a study, including but not limited to: resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments, etc. Oversee SDTM, ADaM and TLF development, perform Senior Review of outputs. Liaise with other Sponsor departments for additional programming needs, as required to support publications, medical writing and additional development needs and analyses. Support/oversee submission activities (especially in late phase team). Ensure all activities are conducted efficiently, with appropriate set-up of needed tools and macros, prioritizing quality at all times. Mentor less-experienced team members in best practices around SDTMs, ADaMs and TFLs while ensuring adherence to department standards and processes. Your Profile: Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company. Solid experience with complex clinical trials (minimum 5 years) and the corresponding data sets content (safety and efficacy) and endpoints. Ideally you will have knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management. Expert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programs. Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, Reviewer's Guides and submission standards. An autonomous, collaborative work style, a curious mind and a keen attention to detail. Fluency in English – both verbal and written – is a must. Learn more about our EEO & Accommodations request here .