Talentify.io
Statistical Analyst ( Remote Opportunity available)
Talentify.io, Little Ferry, New Jersey, us, 07643
Employer Industry:
Pharmaceutical
Why Consider This Job OpportunitySalary up to the maximum amount specified by the companyComprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)Eligibility for short-term incentive programsOpportunity for career advancement and growth within the organizationChance to work on innovative medicines and solutions that make a positive impact on people's livesSupportive and inclusive work environmentWhat To Expect (Job Responsibilities)Lead statistical programming activities for routine studiesDevelop SAS programs for ADaM data sets following CDISC standardsCreate Tables, Listings, and Figures using SAS programsValidate ADaM data sets and Tables, Listings, and FiguresCreate documentation for regulatory filings and participate in the development of standard SAS MacrosWhat Is Required (Qualifications)MS in Statistics, Computer Science, or related field with 3+ years of relevant experience, OR BS in Statistics, Computer Science, or related field with 5+ years of relevant experiencePractical understanding of SAS programming concepts and techniques related to drug developmentBasic understanding of CDISC Standards and drug development processClear communication skills both oral and writtenHow To Stand Out (Preferred Qualifications)Experience with drug development processesKnowledge of additional programming languages such as R or PythonFamiliarity with clinical trial data analysis
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Pharmaceutical
Why Consider This Job OpportunitySalary up to the maximum amount specified by the companyComprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)Eligibility for short-term incentive programsOpportunity for career advancement and growth within the organizationChance to work on innovative medicines and solutions that make a positive impact on people's livesSupportive and inclusive work environmentWhat To Expect (Job Responsibilities)Lead statistical programming activities for routine studiesDevelop SAS programs for ADaM data sets following CDISC standardsCreate Tables, Listings, and Figures using SAS programsValidate ADaM data sets and Tables, Listings, and FiguresCreate documentation for regulatory filings and participate in the development of standard SAS MacrosWhat Is Required (Qualifications)MS in Statistics, Computer Science, or related field with 3+ years of relevant experience, OR BS in Statistics, Computer Science, or related field with 5+ years of relevant experiencePractical understanding of SAS programming concepts and techniques related to drug developmentBasic understanding of CDISC Standards and drug development processClear communication skills both oral and writtenHow To Stand Out (Preferred Qualifications)Experience with drug development processesKnowledge of additional programming languages such as R or PythonFamiliarity with clinical trial data analysis
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