Senior Statistical Programmer
SENIOR STATISTICAL PROGRAMMER REQUIREMENT #12-00157 RECRUITER: BRIDGET BURNS JOB LOCATION: BASKING RIDGE, NJ JUNE 21, 2012 PROJECT DESCRIPTION: A statistical programmer provides timely support to the study team on all programming matters according to the project strategies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. Should have the ability to generate all of the production tables needed for a given study, and to work with other programmers and statisticians in providing a quality review of the results. Must follow SOPs and department work instructions with a minimum amount of supervision. Has the ability to work on multiple projects and maintain timelines. Knowledge of SAS (Base, Macro, Stats) required, and knowledge of the FDA is desirable, Production programming experience is also a plus. RESPONSIBILITIES: • Oversees the ad hoc as well as production programming for three to four clinical studies. • Provides timely support to the study team on all programming matters according to the project strategies. • Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines • Implements and executes the programming and project standards. • Assists in the design and testing of program logic, coding programs, program documentation and preparation of programs. • Supports ongoing clinical studies requests for statistical and non-statistical analyses. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment. • Ability to support data cleaning effort, and to work with statisticians and data managers. • Ability to support study requirements with challenging timelines under direct supervision of the Associate Director of Statistical Programming. • Support team within a study team involved in the creation and QC of production tables, figures, and listings (TFLs) in support of analysis requirements utilizing Regeneron tools and methodologies. • Follows department SOPs, and Work instructions as well as Server requirements. • Supports the marketing activities for the protocols supported. • Assures that results included in presentation are consistent with results in source /output prior to release. EDUCATIONAL REQUIREMENTS: - Bachelor's or Master's degree required • 2-5 year's experience as a Statistical Programmer TECHNICAL SKILLS: Clinical SAS Programmer responsible for creating tables, listings, figures and analysis data sets. Consultant should have at least 3 years of clinical SAS experience working in the Biostatistics department. Good understanding of Analysis Data Sets and Procs. Experience with STDM, using CDISC, and/or ADaM programming is a plus, but not required. SAS, S-Plus (or R), JMP, and MS Office. Knowledge of FDA requirements is desirable. Ability to work in fast-paced environment is required. CORE COMPETENCIES: • Must be able to work in a consistently busy environment. • Flexibility and multi-tasking are highly desirable skills for this position. • Written and oral communication skills This 6+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Bridget: [Click Here to Email Your Resumé] Requirements Bachelor’s or Master’s degree required, 2-5 year’s experience as a Statistical Programmer, 3 years of clinical SAS experience
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