ShiftCode Analytics
Senior / Lead Statistical Programmer : Takeda
ShiftCode Analytics, Boston, Massachusetts, us, 02298
candidate has 12+ years of experience
Visa: all ( no h1b/ opt /cpt)
hybrid...
JD: 8+ years of pharmaceutical industry sas programming experience
Looking 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 standards Perform data manipulation, analysis and reporting of clinical trial data Create analysis files, tables, listings, and figures and validation of those files Maintain project tracking and validation documentation Work well in an environment where team members may be distributed across multiple locations Review planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy and completeness of programming requirements Present statistical programming concepts to non-programming team members as necessary Collaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and priorities Serve as back-up to Principle Statistical Programmer as needed Basic 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 experience Prior regulatory submission and response experience Excellent analysis and reporting skills Experience with ISS/Client Experience with Macro development Command of drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data Knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards In depth knowledge of SAS Graph and Stat packages Familiarity 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 standards Perform data manipulation, analysis and reporting of clinical trial data Create analysis files, tables, listings, and figures and validation of those files Maintain project tracking and validation documentation Work well in an environment where team members may be distributed across multiple locations Review planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy and completeness of programming requirements Present statistical programming concepts to non-programming team members as necessary Collaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and priorities Serve as back-up to Principle Statistical Programmer as needed Basic 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 experience Prior regulatory submission and response experience Excellent analysis and reporting skills Experience with ISS/Client Experience with Macro development Command of drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data Knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards In depth knowledge of SAS Graph and Stat packages Familiarity 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