Medical Safety Director

Há 1 mês


Lisboa, Lisboa, Portugal IQVIA Tempo inteiro

Safety Oversight and Expertise

We are seeking a Medical Safety Director to provide medical, scientific, and therapeutic expertise on pharmacovigilance services. As a key member of our team, you will participate in all aspects of Medical Safety activities, including reviewing and clarifying trial-related Adverse Events, and providing medical evaluation of post-marketing adverse drug reactions.

Key Responsibilities:

  1. Perform medical review and clarification of trial-related Adverse Events and post-marketing adverse drug reactions.
  2. Conduct safety aggregate report reviews and provide medical inputs for signal management and benefit-risk evaluation.
  3. Represent safety and clinical data review findings during client meetings.
  4. Provide medical review and edits to various reports and plans.

Requirements:

  • Medical degree from an accredited and internationally recognized medical school.
  • Three years of clinical practice experience with two additional years in the pharmaceutical or associated industry.
  • Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research, including safety and good clinical practice.

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