Clinical Trials Medical Director

6 days ago


Bloemfontein, Orange Free State, South Africa IQVIA Full time

About Us:

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Job Responsibilities:

  • Aggregate reviews of safety information, including clinical data, to maintain oversight of a product's safety profile.
  • Lead signal detection and analysis, including signal detection strategy, frequency, and timing.
  • Provide medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports.
  • Provide medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies.
  • Review and contribute to benefit-risk evaluation of drugs in clinical trial and post-marketing set up.
  • Provide safety oversight and contribution for label development, review, and updates.
  • Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document.


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