Hi,
Please help to fill below requirement:- SAS Programmer - Phase IV Wilmington DE. 6 month + contract $60/hr corp to corp *face to face interview* I have a new on site 6 month + contract opening with a Pharmaceutical company in Wilmington DE. They are looking for a SAS programmer to do Phase IV work, but said that experience wasn’t necessary coming into the project, so someone who has done more mainstream Phase II and III Trial work would suffice. Candidates need to be within driving distance for a face to face interview. Please only send me your candidates, no partner companies or candidates you sourced off the boards. Rate target is 60/hr corp to corp. The description is below. Our client has an immediate opening for a Statistical Programmer who will work within the Biostatistics Dept for the Scientific Communications team (Phase IV), in exploratory data analyses and data queries as requested by medical affairs, marketing, or the pharmacovigilance group. Main responsibilities: • Work with statisticians to conduct and/or validate analyses of clinical/non-clinical data for scientific meeting presentations, publications and medical information flyers. • Support processes for traceability and reproducibility of publications in a dynamic and multi-task working environment. • Provide analytical programming support for external academic collaborators as needed • Build and maintain integrated safety databases (‘data warehouses’) for monitoring and safety queries • Derive and maintain key analysis datasets and corresponding data specification documents in the standard study environment Occasionally, the analyst will also engage in: • Analyses for internal Quarterly Safety Reviews (QSRs) • Conduct additional analyses that may be needed for formulary submission dossiers and other health economic outcome research tasks. • It is anticipated that this newly created position will also support the Executive Director in introducing and using software for safety signal detection of internal clinical studies. Requirements • M.S. degree in statistics, MPH, or related field. • A minimum of 3 years of experience in the pharmaceutical or biotechnology industries with knowledge of statistical programming related to clinical and non-clinical data in the industry • Strong SAS programming skills in data step manipulation, macro language and major statistical procedures • In-depth knowledge in the following areas would be considered a plus: • Familiarity with publication process. • Experience in accessing and analyzing large databases for safety signal detection. • Knowledge of analyzing high dimensional data (e.g. cluster analysis, heat maps, factor analysis). • Experience in data mining techniques *Sam (Saurabh Gaur)* *Sage Group Consulting Inc.* *Direct Number*: *732-784-6489* *Office: 732-767-0010 Extn: 604* -- *Please only reply to my official ID sg...@sagetl.com <sg...@sagetl.com>* Sam (Saurabh Gaur) Sage Group Consulting Inc. Office: 732-767-0010 Extn: 604 Email: sg...@sagetl.com GTalk: superbsam21 | Yahoo: saurabh_gaur www.sageci.com [image: Description: saplogoone][image: SageLogoC] -- You received this message because you are subscribed to the Google Groups "SRAOSS REKS" group. To unsubscribe from this group and stop receiving emails from it, send an email to sraoss-reks+unsubscr...@googlegroups.com. To post to this group, send email to sraoss-reks@googlegroups.com. Visit this group at http://groups.google.com/group/sraoss-reks. For more options, visit https://groups.google.com/d/optout.
