Hi There, Please let me know your interest for below position and kindly send an updated resume along with the contact details and expected rate.
*Position: *Fusion Middleware Developer *Location: *Sacramento, CA *Period*: January 15, 2010 through January 14, 2011 *CLIENT: STATE GOVT OF CA* * * *Skills: **Oracle Fusion Middleware Suite, **HTB, mid-to-large solution, Business-to-Business (B2B),Service Oriented Architecture (SOA),HL7,Oracle Fusion Middleware, Initiate eMPI, and Orion Concerto Portal, Clinical Data Repository,*** *Mandatory Qualifications: * 1. Experience implementing HTB in a mid-to-large solution (i.e., 1000 users or more); 2. Experience implementing Business-to-Business (B2B) and Service Oriented Architecture (SOA) solutions using Health Level 7 (HL7) and HTB; and 3. Experience implementing Oracle Fusion Middleware, Initiate eMPI, and Orion Concerto Portal within a single integrated environment. * * *Desirable Qualifications: * 1. Experience with CLIENT’S Clinical Data Repository implementation or an equivalent project; 2. Understanding of the state budget process; 3. Experience with projects supporting health care environments; 4. Experience deploying enterprise technology solutions within a health care and/or correctional environment; 5. Ability to work in a team environment as well as independently. *Scope of Services:* 1. Oracle Fusion Middleware Suite support to develop SOA services that interact with Clinical Forms Server and populate data in the HTB intake table. Activities may include, but are not limited to, designing, developing, testing, and deploying of services using Oracle's SOA Suite components (e.g., BPEL, ESB, OWSM, BAM, and Business Rules Engine server); 2. Perform as a single point-of-contact for CLIENT' Clinical Documentation project; 3. Provide input with other project team members for maintenance of overall project schedule(s) and plan(s); 4. Work collaboratively with DCIO and other project staff to ensure CDR-related systems meet CLIENT requirements, and system/business processes are acceptable to CLIENT; 5. Collaborate with staff members to identify issues and risks, maintain issue log(s), provide prompt attention to, and resolution of, issues and escalate when necessary; 6. Assist with preparation of issue, decision, and research documents (i.e., memorandums); 7. Participate in CDR project/team meetings, as necessary, and assist with proceedings; 8. Assist project managers with logistics, planning, documentation, and review of products; 9. Prepare monthly status reports and ensure that all information involving clinical documentation is provided to CLIENT’ DCIO; 10. Complete services in agreed upon timeframe including a weekly status report to the DCIO describing current project status, services produced during previous month, plans for upcoming month, and any issues and/or risks identified during reporting period; and 11. Participate in coordination meetings, providing CDR subject matter expertise, gather required information, and make recommendations, as appropriate. · The consultant(s) will actively participate in information gathering meetings, fact-finding meetings, working sessions, status reporting (both verbal and written), presentations, and general communication(s) on an ongoing basis to help ensure success of the project. -- Thanks and Regards Prashanth CELERSYSTEMS Work: 916-458-5575 Email: prasha...@celersystems.com IM: prashanth_rec (Yahoo) Gtalk: Prashanth.rec -- You received this message because you are subscribed to the Google Groups "SAP Workflow" group. To post to this group, send email to sap-workf...@googlegroups.com. To unsubscribe from this group, send email to sap-workflow+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/sap-workflow?hl=en.
