Clinical Database Management Professional II

Clinical Database Management Professional II #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pharmaindustry #doctor #phd #oncology #drugdevelopment #cra #biotechnology # Review Study protocol and Case Report Forms. Prepare the CRF standards for all phase of studies. Preparation and review of DVS Data Validation specification. Preparation and review of manual listings for the study. Preparation and review of eCRF Completion guidelines for the study. Preparation and review of Time and Event schedule for the study. Creation and review of UAT User Acceptance Testing. Performing UAT User Acceptance Testing of the edit checks for the study. Performing Data Management activities like query management which include, query generation and query resolution. Perform SAE reconciliation and LabVendor data reconciliation. Qualifications M.Sc B.Pharm M. Pharm Function Research & Development Sub Function Biometrics Already Working TEVA If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HRIT partner.