Dear Partners *I have **Keerthi*,* **SAS Developer* *available immediately for your client requirements. Has worked for **AccessPharmaceuticalsInc**, **ICON Clinical Research*, *Amarillo** Biosciences*. *She is in NC right now and is willing to relocate in NC. Please let me know if you have any direct client positions for him. *
*Location: NC* *Relocation: NC* *Availability: ASAP * *Please do send the requirements to **hari...@lightningminds.com*<hari...@lightningminds.com> * **and reach me at* *703-349-5933*** *Please add my ID in your list and send your direct client requirements* * * *SUMMARY:* · Over 8 years of strong experience in SAS and SAS tools emphasizing on analysis, developing, design, testing and implementation of various projects for Pharmaceutical Industries. · Experience in requirement gathering, analysis, planning, designing, coding and unit testing in Windows and Mainframe environments. · Extensive experience in Phase I, II, and III clinical data analysis: analyzing clinical data, creating tables, listing and generating reports and graphs. · Experience in using SAS to read, write, import and export to another data file formats, including delimited files, Microsoft Excel, PDF and access tables. · Experience with SAS Programming and familiar with all phases of Clinical trials. · Experience with clinical trial such as demographics data, adverse event (AE), laboratory data (lab data) and vitals signs. · Experience in analyzing medical claims data and interfacing SAS with MS Office applications such as Access/Excel. · Experience in SAS/BASE, SAS/STAT, SAS/GRAPH, SAS/MACRO, and SAS/SQL. · Proficient in the following reporting, statistical procedures: REPORT, TABULATE, FREQ, MEANS, UNIVARIATE, TRANSPOSE, COMPARE, EXPORT, COPY, CONTENTS. · Experienced in producing HTML, RTF and PDF formatted files using SAS/ODS. · Knowledge of statistical procedures: PROC MIXED PROC MEANS, PROC UNIVARIATE, PROC ANOVA. · Experience in data accessing from relational databases, data analysis and Predictive modeling. *·* Thorough knowledge in preparing Clinical Study Reports by conducting, documenting * *and reporting computer validation inspections in compliance with 21CFR Part 11, FDA regulatory guidelines. · Proven ability to quick learn and apply new technologies. Exceptionally well organized, strong work ethics and willingness to work hard to achieve employer objectives. Clear and concise communication and presentation skills. · Effective team player with an aptitude to learn and ability to prioritize, organize and accomplish multiple tasks, both as part of a team and independently * * *Professional Certification*: SAS Certified Base Programmer for SAS9 *TECHNICAL SKILLS:* SAS Skills: SAS/BASE, SAS/GRAPH, SAS/MACRO, SAS/SQL, SAS/STAT, SAS/ACCESS, SAS/ODS. Operating Systems: Windows 9x/2000, XP, NT, Windows Vista, UNIX Database: Oracle, MS SQL Server, MS-Access, SQL. Others: MS Office, MS Project, Power Point, Excel, SPSS Thanks and Regards *Haritha* *LIGHTNING** MINDS Phone : 703-349-5933 Email: *hari...@lightningminds.com* Web* <hari...@lightningminds.comweb>*: **www.lightningminds.com* -- You received this message because you are subscribed to the Google Groups "KNOW.IT" group. To post to this group, send email to know_it...@googlegroups.com. To unsubscribe from this group, send email to know_it_az+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/know_it_az?hl=en.
