Clinical Database Program(12M) at Plymouth

Job Description

Job Decription:The CDPs Primary tasks include database setup and validation programming within targeted timelines; support the on-going needs for data imports/loads and exports. Also responsible for post-production changes to the database as required. Works closely with Clinical Data Managers and Project Managers and other cross-functional groups; contributes to solutions for routine technical problems of limited scope aligned with specific technical activities and individual and departmental goalsJob Responsibilities Include: Design and create clinical databases within Oracle Clinical, including Remote Data Capture. Database development involves generating the Questions, Question groups, DCMs, DCIs and Character/Graphic layouts. Assist in the development and review of CRF and edit check specifications Review CRF content vs. global library to ensure consistency and standardization within and across databases. Program Validation and Derivation Procedures for study databases Perform alpha testing on the validation and derivation procedures at the time of database release as well as post-production changes Works with the Global librarian or designee to generate any new standard and/or study specific objects. Work with the Clinical affairs project managers to integrate the CTMS system Assist the team by programming/running status reports/metrics using reporting tools (e.g. TOAD, Crystal reports etc.) Develop solutions to basic problems and assists in the development of new technologies Perform quality control of database components Act as subject matter expert to provide technical assistance and training to programming and non-programming personnel Work with databases other than Oracle Clinical if needed for legacy studies Assist in development of data verification audit listings and other audit activities Maintain all required study documentation. Attend study management meetings as necessary Support the team in any study startup and closeout activities including final report data QC Participate in project meetings to give a status update to project managers and upper management. Assist in overall project tasks such as generating CRF completion guidelines, process flowcharts, Standard operating procedures (SOP), work instructions, training guidelines etc. Generate ad-hoc reports as needed.Minimum Requirements: Excellent Oracle Clinical database programming skills Experience with OC Remote Data Capture or other EDC systems preferred Experience with reporting tools (e.g. TOAD, Discoverer, Crystal Reports etc.) Exposure to SAS programming preferred Comply with written procedures, instructions, SOPs and other documents Excellent organizational skills and attention to detail Ability to prioritize and multitask is requiredORL

Job Requirements

 
Country: USA, State: Minnesota, City: Plymouth, Company: InVentiv Health.