Hello Partners, Greetings from *Aim Computer Consulting* We have the following requirement; please revert back to us with 100% matching profiles Only *Send Profiles to: **[email protected]* <[email protected]>
Position :SAS Clinical Trials Programmer Duration :6-9 months Location : Marlborough, MA Rate:45/hr all inclusive This person will be responsible for maintaining the clinical trial DB they are assigned to. Need 1-3 years of clinical trials and SAS programming experience. General Summary: This position is responsible for implementation of SAS programming in support of clinical trials including: generation of patient data listings and reports using SAS; review of tables, listings and reports produced by Biostatistics, and providing programming and biostatistical support to project teams in Clinical Data Management environment. Duties and Responsibilities: o Generate patient data listings and reports using SAS. o Perform validation/quality control check of SAS programs. o Handle SAS programming issues independently, perform independent database and CRF review to ensure programming consistency, and be familiar with all study-programming issues. o Work with Clinical Data Managers, Managers in CDM and Clinical Project Managers to develop listing specifications to meet the project reporting needs and to facilitate efficient data review. o Provide expertise and guidance for Clinical Data Managers regarding listings and reports, and efficiencies that can be gained in data review. o Provide input on the design of CRFs to ensure consistency with protocol and adequacy in collecting data to meet objectives defined in protocol. o Provide expertise to CDM on merging external data with the CRF data and external data processing; participate in establishing processes for these activities. o Support coding processes by providing necessary listings. o Work with Database Programmers and EDC specialists to set up clinical databases. o Review final tables, listings, reports and narratives produced by Biostatistics. o Serve as a liaison between the CDM and Biostatistics. o Review data listings as needed. Minimum Education & Experience: Bachelor's degree in biostatistics, statistics, epidemiology, or public health; Minimum of 1-3 years experience in clinical research and SAS programming; prefer at least 1 year experience in medical device or pharmaceutical industry clinical trials. *Thanks & Regards** * * * *Naga Raj* *Sr. Technical Recruiter* *Aim Computer Consulting* *17197 N .Laurel Park Drive | Suite 513 | Livonia MI 48152* *Phone :** 734-591-3562 EXT 214 | **Fax:** 734-418-2603 * *www.aim-cc.com* <blocked::blocked::http://www.aim-cc.com/>* **|** [email protected]* <[email protected]>* **|** **[email protected]*<[email protected]> * | **[email protected]* <[email protected]> ------------------------------------------------------------------------------------------------------------- Please visit www.NRIYP.com <http://www.nriyp.com/> New generation Yellow pages for NRI’s Classifieds<http://www.nriyp.com/Classifieds/Classifieds_Home1.aspx?Country=> *|* Yellow Pages <http://www.nriyp.com/>* | *Travel<http://www.nriyp.com/Travel/TravelHome.aspx> * | *Classmates <http://www.nriyp.com/Classmates/Classmates_HomePage.aspx> --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [email protected] For more options, visit this group at http://groups.google.com/group/open-source-erp-crm -~----------~----~----~----~------~----~------~--~---
