Quality Analyst I Job in Teva Pharmaceuticals

The opportunity To ensure compliance to good clinical practices, good data management practices, standard operating procedures, protocols, regulatory requirements and applicable principles of good laboratory practices in clinical development, Investigators sites and clinical data base Conducting site audit (approx.: 40% travel), facility and quality system audits Review of clinical development documents generated during study conduct To perform trend analysis and formal review of corrective action and preventive action for clinical monitoring reports and deviations. Preparation & review of standard operating procedures related to the Clinical development and Clinical data management department. Review of protocol, Inform Consent Form and Case Report Form for regulatory compliance Review of clinical study data base design and medical coding. Review of electronic case report form specification, edit check specification, UAT plan & report and to perform user acceptance testing.