Saxon Global
Principle Statistical Programmer (CrossTA-Phase4)
Saxon Global, Phila, Pennsylvania, United States, 19117
ROLE - Principle Statistical Programmer
RATE - $70/hr on C2C
WORK AUTH - All except H1B
LONG TERM CONTRACT - (1-10yrs)
LOCATION - bala cynwyd pennsylvania
JOB DESCRIPTION
A leading global biopharmaceutical company is looking for multiple
Sr. Statistical/Lead/Principle Statistical Programmer
responsible for processing clinical data required for statistical analysis of Phase I - III clinical trials, and leading project teams. We would like to fill this position as soon as possible. 7-10+ years statistical programming experience with pharmaceutical/ CRO industry is required.
Strong Macro Development
experience is required.
PK/PD Programming
is a big plus.
Key ResponsibilitiesProvide 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 neededRequired Qualifications
BA/BSc or Master's in
Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject with 7-8+ years of relevant experienceExtensive
regulatory submission
and response experienceIn depth
SAS Programming
background with excellent analysis and reporting skillsCommand of drug development
life cycle and experience with the manipulation, analysis and reporting of clinical trials dataThorough knowledge of latest
CDISC SDTM, ADaM and Define standardsAbility to effectively oversee geographically diverse programming teamsFamiliarity with other programming languages (e.g. Java, R, or S-Plus)Project management
or project planning experience on small to large scale drug development projectsIn depth knowledge of
SAS Graph and Stat packages
RATE - $70/hr on C2C
WORK AUTH - All except H1B
LONG TERM CONTRACT - (1-10yrs)
LOCATION - bala cynwyd pennsylvania
JOB DESCRIPTION
A leading global biopharmaceutical company is looking for multiple
Sr. Statistical/Lead/Principle Statistical Programmer
responsible for processing clinical data required for statistical analysis of Phase I - III clinical trials, and leading project teams. We would like to fill this position as soon as possible. 7-10+ years statistical programming experience with pharmaceutical/ CRO industry is required.
Strong Macro Development
experience is required.
PK/PD Programming
is a big plus.
Key ResponsibilitiesProvide 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 neededRequired Qualifications
BA/BSc or Master's in
Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject with 7-8+ years of relevant experienceExtensive
regulatory submission
and response experienceIn depth
SAS Programming
background with excellent analysis and reporting skillsCommand of drug development
life cycle and experience with the manipulation, analysis and reporting of clinical trials dataThorough knowledge of latest
CDISC SDTM, ADaM and Define standardsAbility to effectively oversee geographically diverse programming teamsFamiliarity with other programming languages (e.g. Java, R, or S-Plus)Project management
or project planning experience on small to large scale drug development projectsIn depth knowledge of
SAS Graph and Stat packages