The senior/principal biostatisticians will be supporting Phase 2 or 3 studies and be hands-on with data checking, programming, and statistical analysis deliverables under guidance.
Qualifications:
Master's in Statistics, Biostatistics, or related field with 5+ years of experience in the design, analysis, and reporting of clinical studies.
OR
PhD in a related field with 3+ years of experience
Demonstrated experience in SAS programming with a specific emphasis on SAS procedures used in programming statistical analyses commonly used in the analysis of clinical study data.
Significant experience working with CDISC and related FDA standards for specification and creation of SDTM and ADaM datasets.
Numbers & Facts
Location
Remote, NJ (Remote)
Skills
Analysis Skillsunmatched
Biostatisticsunmatched
Clinical Dataunmatched
Clinical Data Interchange Standards Consortium (CDISC)unmatched
Clinical Trialunmatched
Data Analysisunmatched
Data Setsunmatched
FDA (Food and Drug Administration)unmatched
Statistical Analysis System (SAS)unmatched
Statistical Programming Languagesunmatched
Statisticsunmatched
🎯
Be found by employers
5,500+ employers search our resume database daily. Add yours to get found by recruiters looking for candidates like you.
Level up your application
Professional resume templates
Browse dozens of recruiter approved resume templates, layouts and formats. Choose your favorite and make it your own in minutes.