*Hello Folks,* *Kindly find the job description and confirm me with your available candidates on my email id*
*[email protected]* <[email protected]> *Job ID : GSK0JP00049379* *Job Title : Clinical SAS ProgrammerDuration : 18+ Months Location : **RTP (Research Triangle Park), NC* *Job Description:* Functional Title: Clinical Programmer Analyst Core Requirements: Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. This role is centered around the extraction and mapping of data from an in-house standard (called IDSL) to an industry standard format (SDTM). Transformations will primarily be performed through contracted suppliers, and this role will be involved with managing those conversions and keeping data strategy aligned across studies & projects. An understanding of all required SDTM components is essential, including the clinical domains, TDDs, Data Reviewers Guide, define.xml and aCRF. Some programming experience with SAS is required, but the position is not primarily a SAS programming role. The ideal candidate will have a background in clinical programming in a data management setting or statistical setting. The ability to focus on customer needs, troubleshooting, and providing innovative technical solutions, while adhering to standards is essential. This is a dynamic position that will require the successful candidate to learn a number of bespoke systems and solutions and implement those effectively in order to deliver a top-notch conversion service. Additional Activities: Support multiple functional groups (i.e. DM, S&P, etc) across all phases Lead SDTM conversion activities across multiple studies concurrently Lead and actively participate in review of SDTM conversion deliverables Create & Maintain process documentation as required Lead or participate in process redesign & optimization SAS programming for creation / review of SDTM domains as required Training of new staff on the role Provide training/guidance on SDTM conversion process for teams Other activities as required to support SDTM conversion and implementation of CDISC standards Additional preferred skills: Experience extracting and transforming clinical data Knowledge of clinical trial processes and supporting systems Strong skills in SQL, PL/SQL. Knowledge of COGNOS and Spotfire beneficial as well. Knowledge of FDA requirements for annotated CRFs Experience with eDC / eDM setup for clinical trials Experience with InForm Architect and Central Designe *Ankur Dixit* Sr. Executive - IT Staffing 240 Cedar Knolls Road, Suite 100 | Cedar Knolls, NJ 07927 Office: 973.967.3434 | Fax: 973.998.2599 Email: *[email protected]* <[email protected]> | Website: *www.artechinfo.com* <http://www.artechinfo.com/> -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" 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/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
