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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Proficient in SAS Programming for clinical data analysis, ensuring compliance with ICH guidelines and CDISC standards. Strong ability to generate analysis datasets, summary tables, and validate programming outputs while managing multiple tasks effectively.
Highest-signal resume keywords
SAS ProgrammingCDISC ComplianceStatistical AnalysisRegulatory Guidelines KnowledgeProject Coordination
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Statistical ProgrammingData AnalysisSAS SoftwareCDISC StandardsADaM DatasetsTLF Shell PreparationValidation ProgrammingSAP PreparationOpenCDISC ReportsAttention to Detail
Soft Skills
Organizational SkillsTime ManagementCommunication SkillsLeadership SkillsAbility to Work Under Pressure
Industry Keywords
Pharmaceutical IndustryICH GuidelinesElectronic Submission StandardsClinical DataStatistical Analysis Plan (SAP)
About the role
Key responsibilities & impact- Conduct statistical programming work of clinical data using SAS Software
- Ensure programs, outputs, and documentation comply with ICH guidelines and company SOPs
- Generate analysis datasets according to CDISC standards and SAP
- Implement analysis methods according to SAP and produce summary tables, graphs, and data listings using SAS
- Conduct ad hoc analyses
- Validate programs and associated results produced by other programming colleagues
- Participate in TLF shell preparation and review
- Assist statistician with SAP preparation
- Run CDISC validation programs, such as OpenCDISC reports, to ensure ADaM datasets are CDISC compliant
- Learn and implement Incyte standard SAS macros for efficient clinical data analyses under Lead Programmer supervision
- Program individual studies independently with minimum supervision
- Check validation summary reports for errors, warnings, and proper SAS program documentation
- Review individual study CDISC validation output
Requirements
What you’ll need- BA/BS degree in mathematics, statistics, computer science or health related field, or equivalent experience
- 4–8 years of SAS programming working experience in the pharmaceutical industry
- Good SAS programming skills and attention to details
- Demonstrated knowledge of regulatory guidelines, including electronic submission standards
- Strong organizational, time management, communication, and project coordination and leadership skills
- Ability to work well under timeline pressure
- Ability to work on multiple tasks while coordinating others at the same time
- Compliance with truthful and complete application information
Benefits
Comp & perks- Incentive plans, bonuses, and/or other forms of compensation may be offered
- Health and welfare benefits may be offered
- Equal opportunity employer