<p> We are working with a medium sized biometric specialist that are scaling up their biometrics team across Europe due to several new partnerships they have formed and looking for Senior and Principal level biostatisticians. </p><p></p><p> My client is able to offer FSP or multi-sponsor studies across various therapy areas and phases. This is a fully remote position, but the candidate must be located in Spain. </p><p></p><p><b> Responsibilities: </b></p><p></p><ul><li> Design, program, and validate complex primary efficacy datasets for clinical studies </li><li> Develop and quality-check summary tables, listings, figures, and statistical analysis outputs in line with SAP requirements </li><li> Collaborate with clients to recommend alternative approaches or supplementary analyses when appropriate </li><li> Create and validate reusable macros to support statistical analyses and graphical outputs </li><li> Conduct Stage 3 quality control reviews to ensure accuracy and compliance </li><li> Provide guidance on complex endpoints and analyses while maintaining consistency across clinical development programs </li><li> Prepare, validate, and review efficacy dataset specifications for individual studies as well as integrated analyses (ISS/ISE)</li><li> Author Statistical Analysis Plans (SAPs), including ISS/ISE SAPs and DSMB SAPs and Charters </li></ul><p></p><p><b> Experience Required: </b></p><p></p><ul><li> Statistics degree or Life Science degree </li><li> Previous experience working as a biostatistician within a CRO or pharmaceutical environment </li><li> Track record of independently leading studies </li><li> Experience working in Oncology is preferred </li><li> Good working knowledge with SAS </li></ul><p></p><p> For more information, please submit your application. </p><p></p><p> Jack Kavanagh </p><p> AL Solutions </p><p></p>