Hi, Greetings!
We have the following client requirement, pl send profiles with rate and contact details ASAP. SAS FDA Regulations Start Date: ASAP Location: Rahway, NJ or West Point, PA 9 yrs experience in SAS , Worked on All phases of Clinical Trial, Knowledge of SDTM, VB, UNIX & C, Clinical Trials data, CDISC, FDA and NDA regulations and standards, Knowledge of MedDra and other dictionaries Position Description: This developer will lead the effort for developing reports to support FDA Standard for Exchange of Nonclinical Data (SEND) pilot project. Developer need to study what has been implemented and developed at Merck SA area. He/She also need to learn SEND format and understand FDA SEND pilot project. The developer should work independently with minimum supervision from Solution Manager. The developer should read SEND requirement and be able to implement the design, development of SEND report. Developer also needs to follow client's SL Immediate interviews for right profiles. Thanks and Regards, Sridhar Ezen Computer Services Inc. 609-945-7416 Fax - 609-452-5613 <mailto:[email protected]> [email protected] <http://www.e-zencomp.com/> www.e-zencomp.com ***Partner to PTC Abortext Products --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "jobinusa" 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/jobinusa?hl=en -~----------~----~----~----~------~----~------~--~---
