.As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies.Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.In this role, you will develop and validate SAS programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team.This position allows you to participate in the development of innovative Oncology drugs. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day.Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!You can be 100% home-based in EMEA or, if you prefer, you can work from our local office in your home country.What else can you expect from us? Rewarding and meaningful work in an established, diverse, highly profitable and respected global company.Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.A genuine work-life balance.Flexibility in working hours.A thorough onboarding with support from your personal mentor.A permanent employment contract with Fortrea.Excellent training and career development opportunities, as well as support with advancing your individual education.Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide.Your responsibilities: Review SAPs and TFL shells from a programming perspective.Advise on the development of complex TFL shells from a programming perspective.Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets.Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs.Produce/define XML/PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs.Respond to QA and client audits and support qualification audits.Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business
