.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. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.Senior Biostatistician (single sponsor)Are you a talented Biostatistician looking for a new opportunity to leverage your skills in a cutting-edge environment? Look no further! At our Biometrics FSPx sponsor dedicated team you will work dedicated to a client specializing in the development of top-level clinical trials within a wide variety of therapeutic areas such as diabetology, cardiovascular, oncology, respiratory, neurological, immunology etc. We are seeking a Senior Biostatistician to join our exceptional team and contribute to groundbreaking research.As a Senior Biostatistician at Fortrea, you will play a crucial role in the design, analysis, and interpretation of clinical trials, directly impacting the development of innovative therapies and treatments. Supported by a diverse team of research professionals, you will collaborate closely with study teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis.Your Responsibilities:* Design and implement statistical strategies for clinical trials within various therapeutic areas.* Develop statistical analysis plans, ensuring their appropriateness for study objectives.* Perform statistical programming tasks using SAS for analyses and generate study reports.* Collaborate with cross-functional study teams to contribute statistical expertise and guidance.* Provide expertise on statistical methodology, sample size calculations, and innovative trial design.* Ensure the quality and integrity of statistical deliverables.Your Skills and Qualifications:* Minimum of 5 years of experience as a Biostatistician within a CRO, biotech or pharmaceutical company.* Solid understanding of statistical methods commonly used in clinical trials, including advanced concepts.* Extensive knowledge of CDISC standards.* Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability todebug SAS programs* Proven professional experience with SDTMs, ADaM datasets and TFLs* Strong knowledge of regulatory guidelines (e.G., FDA, EMA) and industry standards.* Excellent communication skills, with the ability to effectively collaborate and present complex data to non-technical audiences.* Advanced degree (Ph.D. or Master's) in Biostatistics, Statistics, or a related field.* Demonstrated ability to work independently, utilize problem-solving skills, and make sound decisions