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*SAS Programmer* *Location: **Pleasanton, CA* Must have 9-10 years exp Here is requirement details. • Bachelor’s degree, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science. Masters degree in the above fields is strongly preferred. • Experience in working in several different Therapeutic Areas. Experience in the medical device field/ diagnostics preferred • 5-10 years SAS Base programming, with minimum of 4 year using SAS/ STAT, SAS/GRAPH and SAS/MACRO. • At least 5 years relevant experience in the pharmaceutical, biotechnology industry or CRO • Experience of data extraction process and ability to import and extract data from databases or data warehouses into SAS system. Ability to develop specifications for development of standardized code for repeated processes. • Experience in developing appropriate processes for quality control (QC) of programs across all phases of clinical trials. Extensive experience of quality control processes and methods. • Knowledge and experience programming for submissions to Center for Devices and Radiological Health division of FDA and to other regulatory authorities in the world preferred. • Experience of handling complex programming and data issues. Knowledge and ability to apply good clinical practices, and 21 CFR part-11 in clinical and statistical programming assignments. Ability to act as a liaison between biostatistician and programmers working on study for addressing complex data and programming issues. • Experience of developing statistical reports, patient profiles, and ad-hoc reports based on specifications in analysis plan. • Effective communication and interpersonal skills • Ability to creates tables, listings, and graphs from specifications developed in conjunction with study statistician or support programming staff for safety, efficacy and for pooled data reporting/ integrated summaries of safety and efficacy • Familiarity with Investigational Device Exemption (IDE) specific submission processes. Experience with IDE submission is strongly preferred. • Knowledge of CDISC data standards, including CDASH and Submission Data Standards, ADaM experience or demonstration of knowledge in these areas is a plus. Experience of working on define.xml is strongly preferred. -- *Thanks,* Nicole Xie *Office: (908) 429-8008 x315* *Cell: (908) 256-2714 * www.cyberThink.com/staffing <http://www.cyberthink.com/staffing> Click here to view current job openings. <http://www.maxhire.net/cp/?E95E6C361D43515B7E511F29> [image: Description: Description: Description: cid:[email protected]] *Connecting with the best and brightest is our goal, please ask about our referral bonus policy.* -- You received this message because you are subscribed to the Google Groups "it req" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/it-req. For more options, visit https://groups.google.com/d/optout.
