Talentify.io
Senior Statistical Analyst (Remote) - Pipeline
Talentify.io, Little Ferry, New Jersey, us, 07643
Employer Industry:
Pharmaceutical Research and Development
Why Consider This Job OpportunitySalary up to $CompetitiveOpportunity for career advancement and growth within the organizationComprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)Participation in short-term incentive programsRemote work flexibility within the USChance to work on innovative medicines and solutions that impact people's livesWhat To Expect (Job Responsibilities)Lead statistical programming activities for projects and studies with lower complexityCreate documentation for regulatory filings and develop standard SAS MacrosProvide oversight and mentoring to assigned Statistical Programmers and AnalystsDevelop SAS programs for ADaM data sets and Tables, Listings, and FiguresValidate ADaM data sets, Tables, Listings, and FiguresWhat Is Required (Qualifications)MS in Statistics, Computer Science, or related field with 5+ years of relevant experience OR BS with 7+ years of experienceProficiency in SAS programming and CDISC StandardsUnderstanding of drug development process and regulatory filingsClear communication skills, both oral and writtenAbility to estimate effort required for study-related programming activitiesHow To Stand Out (Preferred Qualifications)Experience working in pharmaceutical research or a related fieldFamiliarity with other statistical programming languages
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Pharmaceutical Research and Development
Why Consider This Job OpportunitySalary up to $CompetitiveOpportunity for career advancement and growth within the organizationComprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k)Participation in short-term incentive programsRemote work flexibility within the USChance to work on innovative medicines and solutions that impact people's livesWhat To Expect (Job Responsibilities)Lead statistical programming activities for projects and studies with lower complexityCreate documentation for regulatory filings and develop standard SAS MacrosProvide oversight and mentoring to assigned Statistical Programmers and AnalystsDevelop SAS programs for ADaM data sets and Tables, Listings, and FiguresValidate ADaM data sets, Tables, Listings, and FiguresWhat Is Required (Qualifications)MS in Statistics, Computer Science, or related field with 5+ years of relevant experience OR BS with 7+ years of experienceProficiency in SAS programming and CDISC StandardsUnderstanding of drug development process and regulatory filingsClear communication skills, both oral and writtenAbility to estimate effort required for study-related programming activitiesHow To Stand Out (Preferred Qualifications)Experience working in pharmaceutical research or a related fieldFamiliarity with other statistical programming languages
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