Title: Oracle Clinical Programmer/ Data Manager Work Location: NJ
Duration: 6 months Rate: $75/hr Overview We are seeking an Oracle Clinical Programmer/ Data Manager who will work with Ad Hoc SAS Programmers, Integrated Review Administrator, OC DBA, Manager, Database Administration and CRF designer to meet the needs of various customers. Responsibilities: . Building and designing clinical studies in Oracle Clinical (OC) in concert with Data Managers; use PL/SQL Programming to develop Ad Hoc reports, OC procedure programming; OC study planning, design and standardization. . Work with the Integrated Review administrator to deploy Ad Hoc SQL reports/SQL code to users via integrated review. . Documentation, development and maintenance of the OC Global Library according to agreed upon standards. . Providing assistance to Data Managers in ensuring that CRFs are compatibly designed with OC standards. . Interaction with SAS Programmers in standardization of SAS Data Structures. . Maintenance of OC and TMS administrative reference code lists. . Creation and documentation of DCMs, DCIs and workbooks for clinical studies. . Creation and programming of OC validation and derivation procedures including documentation and testing plan. . Interacting with external vendors concerning external data into OC. . External data loads, and troubleshooting data loads. . OC lab setup including reference ranges, panic flags, unit conversions and Normlab2. . Maintenance and upkeep of study view descriptions and study view templates including extended attributes. . Contribute in refining current Database Administration process as well as revamping and develop old/new processes to increase efficiency. Minimum Qualifications and knowledge: . Five or more years experience in Oracle Clinical, with at least two years in a database programming capacity. . In depth experience with Oracle Clinical database design, PL/SQL. . Degree in life sciences, MIS, pharmacy or nursing; advanced degree desirable. . Formal or on the job training in clinical trial methodology and Good Clinical Practice (GCP). . Good organizational and project/time management skills. . Team player who can interact effectively with the SAS Programming, data management and clinical departments. . Ability to listen and understand the customer's needs Additional Desirable Qualifications: . Oracle Clinical/TMS validation experience. . Familiarity and working knowledge of Oracle Clinical/TMS underlying database tables. . Knowledge and experience in Oracle Clinical add-ons such as Integrated Review and/or Oracle Discoverer and query tools. -- Regards, krish mylangam, kri...@gdninfo.net. 317-8636-0721 --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To post to this group, send email to open-source-erp-crm@googlegroups.com To unsubscribe from this group, send email to open-source-erp-crm+unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/open-source-erp-crm -~----------~----~----~----~------~----~------~--~---
