SENIOR STATISTICAL SAS PROGRAMMER (DG)

SENIOR STATISTICAL SAS PROGRAMMER (DG)

 

Full-time Senior Statistical SAS Programmer Major Pharmaceutical firm, Salary up to $100,000 base + bonus depending on experience.  Company is easily accessible from most locations in Central and North NJ. 

 

In this role you will be responsible for the following:All programming aspects which include, pooled datasets, analysis datasets, listings and tables of individual clinical trials phases I through IV and project level activities for small drug projects and indications. Lead programming activities for a trial, early phase project indication or publication activities.  Lead large complex projects under supervision of a Statistician or Director. Maintain efficient interfaces with internal and external customers with support of management and Statisticians. Develop resource plans as required with support of the Director. Develop and comply with project study standards and specifications following internal guidelines. Confirm that documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structure tables, listings and figures for phase I through IV clinical trials and submission activities. Program according to specifications, analysis datasets, pooled datasets, pooled datasets, listings, tables, and figures for phase I through IV clinical trials. Work with the statistician to develop specifications for analysis datasets, pooled datasets, and listings. Support QC and QA of deliverables. Maintain records for all assigned projects and archiving of trial project analysis and associated documentation. Participate in the selection of CROs and supervise the Statistical reporting trial activities of the CROs. Provide input on process improvement initiatives and participate in non-clinical project activities.

 

Requirements:BA or BS in mathematics, statistics, computer science or life sciences or other related field.Intermediate knowledge of and experience with SAS software. Fluent in English (oral and written).Working knowledge of database design structures. Good understanding of global clinical trial practices, procedures, methodologies. Good understanding of regulatory requirements relevant to Statistical Reporting (GCP & ICH). Good knowledge of office tools. Must have at least 4 years experience in a SAS programming role supporting clinical trials in the pharmaceutical industry.2 years for MS Statistics or Computer Science graduates.Must have a green card or be a US citizen to apply. 

 

Please send your resume in Word format Darren Gutowski at dgutowski@clarkdavis.com ; CLARK DAVIS ASSOCIATES, 5 Century Drive, Parsippany, NJ, 07054; Phone (973) 267-5511; Fax (973) 267-0232



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