Principal biostatistician – leading cro – homebased – spain we have recently partnered with an award winning cro, who are looking for an experienced principal statistician (or senior looking to move into principal), to join their successful study delivery team, any area of specialism considered how you will be a success: as a principal biostatistician, you will be accountable for: - leading biostatistics and programming activities for a program of studies with moderate complexity and/or high value and impact for the organization. - planning, monitoring, organizing, and reviewing activities of biostatisticians and programmers working on the assigned program of studies. - ensuring the timely, budget-compliant delivery of individual studies and integrated analyses to the required quality standards. - maintaining consistency across studies within the program. - providing strategic oversight and direction, with a focus on optimal resource allocation and effective team performance. - leveraging your regulatory interaction experience to ensure compliance with regulatory standards and contribute to submissions and responses to regulatory inquiries. desirable experience: - providing biostatistical input into the design of clinical programs, including protocol input such as study design, sample size calculations, and patient randomization schemes. - contributing to statistical aspects of case report form (crf) design. - reviewing project database structures, edit checks, and data management coding conventions. - preparing statistical analysis plans (sap), defining derived data,...
Principal biostatistician – leading cro – homebased – spain we have recently partnered with an award winning cro, who are looking for an experienced principal statistician (or senior looking to move into principal), to join their successful study delivery team, any area of specialism considered how you will be a success: as a principal biostatistician, you will be accountable for: - leading biostatistics and programming activities for a program of studies with moderate complexity and/or high value and impact for the organization. - planning, monitoring, organizing, and reviewing activities of biostatisticians and programmers working on the assigned program of studies. - ensuring the timely, budget-compliant delivery of individual studies and integrated analyses to the required quality standards. - maintaining consistency across studies within the program. - providing strategic oversight and direction, with a focus on optimal resource allocation and effective team performance. - leveraging your regulatory interaction experience to ensure compliance with regulatory standards and contribute to submissions and responses to regulatory inquiries. desirable experience: - providing biostatistical input into the design of clinical programs, including protocol input such as study design, sample size calculations, and patient randomization schemes. - contributing to statistical aspects of case report form (crf) design. - reviewing project database structures, edit checks, and data management coding conventions. - preparing statistical analysis plans (sap), defining derived data,...
Principal biostatistician – leading cro – homebased – spain we have recently partnered with an award winning cro, who are looking for an experienced principal statistician (or senior looking to move into principal), to join their successful study delivery team, any area of specialism considered how you will be a success: as a principal biostatistician, you will be accountable for: - leading biostatistics and programming activities for a program of studies with moderate complexity and/or high value and impact for the organization. - planning, monitoring, organizing, and reviewing activities of biostatisticians and programmers working on the assigned program of studies. - ensuring the timely, budget-compliant delivery of individual studies and integrated analyses to the required quality standards. - maintaining consistency across studies within the program. - providing strategic oversight and direction, with a focus on optimal resource allocation and effective team performance. - leveraging your regulatory interaction experience to ensure compliance with regulatory standards and contribute to submissions and responses to regulatory inquiries. desirable experience: - providing biostatistical input into the design of clinical programs, including protocol input such as study design, sample size calculations, and patient randomization schemes. - contributing to statistical aspects of case report form (crf) design. - reviewing project database structures, edit checks, and data management coding conventions. - preparing statistical analysis plans (sap), defining...
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