*Dear Friend*
*Please find the below job requirement, if you have any consultant for the below position kindly share me the updated resume along with the contact details and expected rate to **si...@datsolinc.com <si...@datsolinc.com>* *Requirement 1:* *Job Title*: SAS Programmers with Pharma and Biostatistics Experience *Location**:* Edison, NJ *Duration**: 6+Months* skills experience Must have skills Understanding of Biostatistics in clinical trial environment 10 Yrs. Biostatistics process and regulatory filings of clinical data downstream from EDC 10 Yrs. Exposure to SAS/SAS DD, “ R” tools for biostatistics 10 Yrs. Understanding of clinical data management processes good to have skills Understanding of clinical data warehousing 2 Years Must have Domain experience Clinical Trials 10 Yrs. *Requirement 2:* *Application Developer* Experience: 6-8 Years *Location*: Milwaukee, Wisconsin *Rate*: Open Job Description · Developer who has 5+ years of experience in client/server application development with focus on delivery and quality. · Experience with different types of testing (Unit, Functional, Integration, Regression, Smoke, Sanity, etc.) · Source code analysis, static code scan, branch versus trunk based development and the strategy around it · Code compilation outside of IDEs · Packaging, delivery and installation into target environments (via Octopus, UrbanCode, home grown automation) · Target environment topology, change management process and auditability · Experience working with Continuous Application Delivery toolsets such as TFS, TeamCity, or UrbanCode Requirement 3 *SAS Business Analyst* *Location*: Groton, Connecticut *Duration*: 3 months and may be extended. *Rate* is as per market standards. *Job Description:* 1. Good understanding of Clinical Trial Space. 2. Good to have but not a must - Experience with SAS and/or understanding of storage on UNIX servers – SAN and NAS. 3. Experience in Analysis & Reporting systems. *Activities involved,* 1. Writing requirements for the four planned items. a. Data Archival from SAN to NAS or using PAST team (approach to be defined during requirements) b. Migration of metadata from current flat files to database. This will allow generation of business metrics which is difficult in flat file systems: Currently there is no dB for CDARS. c. GUI upgrade, including providing users access to archived data through the UI d. SAS 9.4 upgrade 2. Understanding of Clinical terms to come up with way to store metadata such that it can be used be downstream systems in future. 3. Knowledge of HPQC (or HPALM) to update requirements. 4. Possible – help create test cases. *Thanks & Regards,* *Sidhu* *Data **Solutions* *Inc* *** Certified Minority-Owned Business Enterprise (MBE) *** Canton, Michigan 48187 Main - (734) 399-4476 Fax - (734) 437-5524 Email: si...@datsolinc.com <dil...@datsolinc.com> URL: http://www.d atsolinc.com DISCLAIMER: Under Bill 1618 Title III passed by the 105th US Congress this mail cannot be considered Spam as long as we include contact information and a method to be removed from our mailing list. If you have received this message by mistake or are not interested in receiving our e-mails, please reply with a "*REMOVE*" in the subject line and delete this message from your system. We are sorry for the inconvenience caused to you. -- You received this message because you are subscribed to the Google Groups "oraapps" group. To unsubscribe from this group and stop receiving emails from it, send an email to oraapps+unsubscr...@googlegroups.com. To post to this group, send email to oraapps@googlegroups.com. Visit this group at https://groups.google.com/group/oraapps. For more options, visit https://groups.google.com/d/optout.
