*Hi Partners,* ** *Greetings,* ** *Hope you are doing Well!!!!!!!!!!!!!!!* ** *Please forward a profiles to **[email protected]*<[email protected]> ** *Here are the requirement details* **
*Location: *Titusville, NJ *Duration:* 12 months ESSENTIAL FUNCTIONS: (Core Responsibilities) 1. Develop and document programs to create/verify analysis datasets summarizing key clinical trial data. 2. Develop and document programs to produce/verify tables, listings and other reports and analyses summarizing clinical trial results. 3. Perform quality control checks for programs and data 4. Review the protocol, case report forms, and Data Management documents OTHER RESPONSIBILITIES / DETAILED DUTIES: * Review and discuss Statistical Analysis Plan (SAP) and statistical programming specifications. * Create analysis databases and generate analyses and reporting outputs * Demonstrate a good understanding of FDA, ICH and CDISC guidelines * Interact with CROs and review their deliverables as needed * Review programming deliverables from team members if needed. Education: Bachelor’s degree or equivalent in computer science, mathematics or other scientific field (or equivalent theoretical/technical depth). Related Experience: 1. Minimum of 5 years experience programming and analyzing scientific data in a pharmaceutical / clinical trial environment. 2. Expertise in SAS programming language. 3. Experience working in a PC SAS environment . 4. Must have good organization and written and oral communication skills -- Regards, Shankar 248-522-6879 Technology consultanst inc -- You received this message because you are subscribed to the Google Groups "SAP ABAP" 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/sap-abap?hl=en.
