Summary: Must have at least 2 years of clinical data review experience in Clinical Research, review protocol and CRF designs. Adequate knowledge of ICH guidelines. Abstracts all necessary information from Safety Data and recognize data discrepancies in Clinical Database. Performs reconciliation of safety report and clinical patient profile. Post queries for relevant information from safety report to be added in the clinical database. May require narrative writing for clinical data review profile. Quantitative analysis Performs a comprehensive review for the all SAE data but not limited to reported and coded terms. Completes brief description of clinical cases for clinical data review utilizing the autogenerated narratives. Qualitative analysis Ensures all relevant information is captured in clinical database and provides quality , clinically meaningful narratives. Performs all duties according to company policy and regulations and guidance. Performs other duties assigned by the Director or Sr. Manager. No travel required.
Required: - Graduate of adequate health care related course and familiarity with medical terminologies. - Minimum of 1 year of AE/SAE data review in Clinical Research. - Strong knowledge of ICH guideline - Knowledge of INFORM, J -review is a plus and/or other Clinical trial Systems - Proficiency on all related regulations, GCP, and Good Clinical DM Practice Associated topics: diet, dietary, food scientist, health, immuno oncology, immunoassay, nephrology, pharmacometrics, therapy, transfection