Title: Oracle Clinical Programmer/ Data Manager Work Location: Paramus , NJ Duration: 6 months Rate: $82-92/hr C2C
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). · 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. Visit www.itechcp. Best regards, John Barry ITech Consulting Partners 30 Church Hill Road Newtown, CT 06470 203-270-0051 Ext: 301 203-270-0071 Fax john@itechcp. www.itechcp. August 18th - Tues - Reg Mtg 6 pm - Carnevale Center 10 Lenox Ave Pompton Lakes 07442 Rm 009 - bring 20 copies of resume August 25th No Mtg Sept 1 No Mtg - Labor Day Holiday Sept 15th Dinner Mtg - Recruiter Night Out - Bill Belknap Moderator - Beverly Lieberman Halbrecht Lieberman - Joe McComick Clark Davis Oct |
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