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Medical Surveillance Associates

0-3 years
3-5 Lacs P.A.
10 Jan. 17, 2024
Job Description
Job Type: Full Time Education: BDS/ MDS/ BHMS/ BAMS Skills: Interpersonal Skill, Technical Skill

     Interested may reach at - pavan.cm@iqvia.com   

 

  • Reviewing and evaluating adverse event reports (AERs) to determine if they meet regulatory reporting requirements.
  • Entering and maintaining adverse event information in safety databases
  • Narrative writing
  • Communicating with healthcare professionals and other stakeholders to gather additional information about adverse events
  • Assisting in the preparation of safety reports to be submitted to regulatory agencies
  • Monitoring safety literature to stay current on the latest safety information related to the company's products
  • Collaborating with other departments such as clinical research, regulatory affairs, and pharmacovigilance to ensure compliance with safety regulations and guidelines
  • Participating in the development and implementation of safety policies and procedures
  • Reviewing and assessing the safety profile of new and existing products
  • Participating in the development and execution of risk management plans
  • Communicating with regulatory authorities, healthcare professionals, and other stakeholders on safety-related issues.