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259 jobs found for Clinical Sas Programming

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  • Clinical Statistical Programming SAS Programmer Biostatistician Statistics Qualification: M.SC- Statistics or B.SC Statistics ( mandatory ...

  • Clinical Statistical Programming SAS Programmer Biostatistician Statistics Qualification: M.SC- Statistics or B.SC Statistics ( mandatory ...

  • Clinical Statistical Programming SAS Programmer Biostatistician Statistics Qualification: M.SC- Statistics or B.SC Statistics ( mandatory ...

  • Clinical Statistical Programming SAS Programmer Biostatistician Statistics Qualification: M.SC- Statistics or B.SC Statistics ( mandatory ...

  • Clinical Statistical Programming SAS Programmer Biostatistician Statistics Qualification: M.SC- Statistics or B.SC Statistics ( mandatory ...

  • Clinical Statistical Programming SAS Programmer Biostatistician Statistics Qualification: M.SC- Statistics or B.SC Statistics ( mandatory ...

  • Clinical Statistical Programming SAS Programmer Biostatistician Statistics Qualification: M.SC- Statistics or B.SC Statistics ( mandatory ...

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

  • Job Specification :- Working knowledge of database design/structures and basic statistics. Good understanding of global clinical trial project practices, procedures, methodologies. Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). Strong knowledge of / experience

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