Senior Data

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.Puede obtener más detalles sobre la naturaleza de esta vacante y lo que se espera de los solicitantes leyendo la información a continuación.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.Responsibilities:Design, program, and validate complex primary efficacy datasets for clinical studiesDevelop and quality-check summary tables, listings, figures, and statistical analysis outputs in line with SAP requirementsCollaborate with clients to recommend alternative approaches or supplementary analyses when appropriateCreate and validate reusable macros to support statistical analyses and graphical outputsConduct Stage 3 quality control reviews to ensure accuracy and complianceProvide guidance on complex endpoints and analyses while maintaining consistency across clinical development programsPrepare, validate, and review efficacy dataset specifications for individual studies as well as integrated analyses (ISS/ISE)Author Statistical Analysis Plans (SAPs), including ISS/ISE SAPs and DSMB SAPs xcskxlj and ChartersExperience Required:Statistics degree or Life Science degreePrevious experience working as a biostatistician within a CRO or pharmaceutical environmentTrack record of independently leading studiesExperience working in Oncology is preferredGood working knowledge with SASFor more information, please submit your application.Jack KavanaghAL Solutions

This is a fully remote position, but the candidate must be located in Spain.Responsibilities:Design, program, and validate complex primary efficacy datasets for clinical studiesDevelop and quality-check summary tables, listings, figures, and statistical analysis outputs in line with SAP requirementsCollaborate with clients to recommend alternative approaches or supplementary analyses when appropriateCreate and validate reusable macros to support statistical analyses and graphical outputsConduct Stage 3 quality control reviews to ensure accuracy and complianceProvide guidance on complex endpoints and analyses while maintaining consistency across clinical development programsPrepare, validate, and review efficacy dataset specifications for individual studies as well as integrated analyses (ISS/ISE)Author Statistical Analysis Plans (SAPs), including ISS/ISE SAPs and DSMB SAPs xcskxlj and ChartersExperience Required:Statistics degree or Life Science degreePrevious experience working as a biostatistician within a CRO or pharmaceutical environmentTrack record of independently leading studiesExperience working in Oncology is preferredGood working knowledge with SASFor more information, please submit your application.Jack KavanaghAL Solutions