Senior Clinical Safety Associate Job in Princeton 08540, New Jersey Us
Job Description:This position will be responsible for the collection, documentation and processing immediately reportable events from clinical trials and all adverse events from post marketing spontaneous reports in accordance with Global Pharmacovigilance Regulations and the company’s Standard Operating Procedure. Closely Monitor the safety profile of assigned products, both in development and post-marketing. Actively contributes to the preparation of aggregate and ad hoc safety reports.Qualifications Job Responsibilities· Maintains accurate and complete knowledge of all investigational Read more […]