Senior Statistical Programmer Consultant (remote)

Posted 18 days agoViewed

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💎 Seniority level: Senior, 10 years

📍 Location: United States

🔍 Industry: Pharmaceutical or biotechnology

🏢 Company: ClinChoice

🗣️ Languages: English

⏳ Experience: 10 years

🪄 Skills: Project ManagementSQLData AnalysisSAS EGAlgorithmsData StructuresCommunication SkillsAnalytical SkillsCI/CDProblem SolvingRESTful APIsAttention to detailDocumentationTeamworkCross-functional collaborationData visualizationData modelingData management

Requirements:

Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math or MA/MS with 8 years of experience
Expertise in SAS programming language, report generation, and standards for programming and validation
Experience with CDISC data standards required
Experience as a senior statistical programmer level in a pharmaceutical or CRO working in a FDA regulated environment
Experience with Clinical Study Reports and NDA submission
Ability to work on multiple tasks simultaneously and meet project deadlines
Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment

Responsibilities:

Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings
Produce data listings, summary tables and graphics for interim and final analyses
Integrate data across studies within a project. Test, document, review and validate all programs according to department guidelines
Coordinate data transfer and/or programming standards with CROs and vendors. Validate analysis datasets and TFLs from vendors
Collaborate with other Biometrics functions for all activities related to analyses of clinical trial data
Responsible for execution of ad-hoc requests, manuscripts, posters, and presentations

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