Novartis
Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide.
Job Title: CDS Manager
Job Description:
The CDS & SD Manager evaluates Safety Signals from various sources and keeps the core safety information up-to-date (prepares and reviews CDSs) with current scientific knowledge, including assessments and recommendations made public by regulatory authorities. Ensures patient safety through timely and adequate updates of the core safety in-formation of marketed products. Tracks signals in the signal management tracking system, and evaluates line listings and safety information in scientific literature, including reference product information and regulatory authority communication. Works closely with affiliates to harmonize labelling, periodically collect compliance information and prepare management reports. Prepares, and drives timeliness, volume and high quality of CDS documents Assists in managing 3rd party providers for the production of CDS and other documents. Prepares data packages required by 3rd party providers. Reviews and qualifies CDSs deliveries from providers Health Care Professional with labelling and ideally regulatory background, i.e., Pharmacist, PharmD, MD and equivalent Fluency in English, including medical / pharmaceutical terminology. Familiarity with EU signal sources / regulatory bodies At least 1 year of experience in drug safety/development or closely
related areas of responsibility Experience of safety document writing Good negotiation, proactive and performance oriented, project management and communication skills Fluency in EU and US regulationQualifications:
Health Care Professional with labelling and ideally regulatory background, i.e., Pharmacist, PharmD, MD and equivalent Fluency in English, including medical / pharmaceutical terminology. Knowledge of other languages desirable and necessary Established knowledge of, and experience in the EU drug regulatory environment and drug approval procedures Familiarity with EU signal sources / regulatory bodies At least 1 year of experience in drug safety/development or closely related areas of responsibility Experience of safety document writing Good negotiation, proactive and performance oriented, project management and communication skills Fluency in EU and US regulation
