Drug Safety Associate Job in Raritan 08869, New Jersey US
Drug Safety Associate IIIResponsible for participating in the collection, safety review, processing and reporting of adverse events data in compliance with applicable FDA and global regulations and Janssen AI Standard Operating Procedures (SOPs) and guidelines.Major Duties and Responsibilities:• Processes adverse event information received by the GPRM department for assigned products, and assists in the preparation of internal and external reports.o Triages incoming cases to determine seriousness for processing and reporting prioritizationo Reviews case information for appropriate distribution Read more […]
April 3, 2007
• Tags: Drug Safety Associate Job in Raritan 08869, New Jersey Us • Posted in: General • Comments Off on Drug Safety Associate Job in Raritan 08869, New Jersey US