Monitors the clinical safety of projects /products including activities such as literature review, evaluation of individual cases or signal detection, and responds to safety related questions appropriately .
Performs medical assessment and related activities for cases whenever required, including collecting additional follow-up information as necessary, medical evaluation of product quality defects with adverse events, review of line listings of single cases, and preparation of investigator notifications and periodic medical assessments for ethics committees.
Identifies safety signals based on the review of solicited or unsolicited single cases.
Performs signal detection, monitoring and evaluation of all safety signals.
Provides inputs into responses to inquiries from regulatory authorities or health care professionals on safety issues.
Prepares safety data for Health Authority review boards.
Provides inputs to responses for legal queries and Country Organization requests involving safety issues.
Provides expert evaluation on the clinical context of adverse event reports, assessment of the medical conditions, and the implications on Novartis products.
Collaborates productively on clinical safety tasks with colleagues from Clinical Development, Regulatory Affairs, Medical Affairs, Medical Information, Statistics, Safety Data Management, Epidemiology and other related departments.
Contributes to the development of departmental goals and objectives.
Distribution of marketing samples (where applicable)
Key Performance Indicators
Timeliness and quality of safety analyses, interpretations, and presentations -Compliance with internal and external regulations and procedures -Compliance, consistency and quality of safety deliverables
