ShiftCode Analytics
Senior / Lead Statistical Programmer : Takeda
ShiftCode Analytics, Boston, Massachusetts, us, 02298
candidate has 12+ years of experienceVisa: all ( no h1b/ opt /cpt)hybrid...JD: 8+ years of pharmaceutical industry sas programming experienceLooking for Sr. Statistical Programmer or Principle Statistical Programmer with
8-10+ years experience . Required previous experience working with Phase IV (Post-Marketing) trial; detailed on the resume.
Provide quality deliverables by following corporate and departmental policies, procedures and applicable standardsPerform data manipulation, analysis and reporting of clinical trial dataCreate analysis files, tables, listings, and figures and validation of those filesMaintain project tracking and validation documentationWork well in an environment where team members may be distributed across multiple locationsReview planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy and completeness of programming requirementsPresent statistical programming concepts to non-programming team members as necessaryCollaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and prioritiesServe as back-up to Principle Statistical Programmer as neededBasic Qualifications
BA/BSc in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject with at least 8-10+ years of pharmaceutical industry SAS Programming experiencePrior regulatory submission and response experienceExcellent analysis and reporting skillsExperience with ISS/ClientExperience with Macro developmentCommand of drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials dataKnowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standardsIn depth knowledge of SAS Graph and Stat packagesFamiliarity with other programming languages (e.g. Java, R, or S-Plus)
Search Terms:
SAS Programmer, Clinical SAS Programmer, Statistical Programmer, Sr. Statistical Programmer, Pharmaceutical SAS Programmer, Principle Stat Programmer
8-10+ years experience . Required previous experience working with Phase IV (Post-Marketing) trial; detailed on the resume.
Provide quality deliverables by following corporate and departmental policies, procedures and applicable standardsPerform data manipulation, analysis and reporting of clinical trial dataCreate analysis files, tables, listings, and figures and validation of those filesMaintain project tracking and validation documentationWork well in an environment where team members may be distributed across multiple locationsReview planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy and completeness of programming requirementsPresent statistical programming concepts to non-programming team members as necessaryCollaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and prioritiesServe as back-up to Principle Statistical Programmer as neededBasic Qualifications
BA/BSc in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject with at least 8-10+ years of pharmaceutical industry SAS Programming experiencePrior regulatory submission and response experienceExcellent analysis and reporting skillsExperience with ISS/ClientExperience with Macro developmentCommand of drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials dataKnowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standardsIn depth knowledge of SAS Graph and Stat packagesFamiliarity with other programming languages (e.g. Java, R, or S-Plus)
Search Terms:
SAS Programmer, Clinical SAS Programmer, Statistical Programmer, Sr. Statistical Programmer, Pharmaceutical SAS Programmer, Principle Stat Programmer