Pharmacovigilance

Roles & Responsibilities of Pharmacovigilance A Drug Safety Associate is a professional who works in the field of pharmacovigilance within a pharmaceutical, biotechnology, medical company or life sciences consulting firm. The main role of a Drug Safety Associate is to monitor the safety of drugs and medical devices once they are on the market and ensure that they are being used safely. Reviewing and evaluating adverse event reports (AERs) to determine if they meet regulatory reporting requirements.Entering and maintaining adverse event information in safety databasesNarrative writingCommunicating with healthcare professionals and other stakeholders to gather additional information about adverse eventsAssisting in the preparation of safety reports to be submitted to regulatory agenciesMonitoring safety literature to stay current on the latest safety information related to the company's productsCollaborating with other departments such as clinical research, regulatory affairs, and pharmacovigilance to ensure compliance with safety regulations and guidelinesParticipating in the development and implementation of safety policies and proceduresReviewing and assessing the safety profile of new and existing productsParticipating in the development and execution of risk management plansCommunicating with regulatory authorities, healthcare professionals, and other stakeholders on safety-related issues.Job Types: Full-time, Permanent, Fresher Compensation: 25,064.34 - 35,471.11 per month Benefits: Health insurancePaid sick timeProvident FundWork Location: In person .